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WO2021069575A1 - Heteroaryl-substituted pyrazine derivatives as pesticides - Google Patents

Heteroaryl-substituted pyrazine derivatives as pesticides Download PDF

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Publication number
WO2021069575A1
WO2021069575A1 PCT/EP2020/078261 EP2020078261W WO2021069575A1 WO 2021069575 A1 WO2021069575 A1 WO 2021069575A1 EP 2020078261 W EP2020078261 W EP 2020078261W WO 2021069575 A1 WO2021069575 A1 WO 2021069575A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
optionally substituted
group
spp
c4alkyl
Prior art date
Application number
PCT/EP2020/078261
Other languages
French (fr)
Inventor
Andreas Turberg
Iring Heisler
Joachim Telser
Alexander ARLT
Peter Jeschke
Hans-Georg Schwarz
Martin FÜSSLEIN
Yolanda Cancho-Grande
Peter Loesel
Ulrich Ebbinghaus-Kintscher
Bing Ashley Liang O'DOWD
Arunas DAMIJONAITIS
Steffen Müller
Jiakang MA
Original Assignee
Bayer Animal Health Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/CN2019/110528 external-priority patent/WO2021068179A1/en
Application filed by Bayer Animal Health Gmbh filed Critical Bayer Animal Health Gmbh
Priority to US17/766,151 priority Critical patent/US20230023326A1/en
Priority to CA3156083A priority patent/CA3156083A1/en
Priority to JP2022521165A priority patent/JP2022550996A/en
Priority to CN202080085776.1A priority patent/CN114761393A/en
Priority to AU2020362341A priority patent/AU2020362341A1/en
Priority to BR112022006753A priority patent/BR112022006753A2/en
Priority to MX2022004192A priority patent/MX2022004192A/en
Priority to KR1020227015626A priority patent/KR20220080159A/en
Priority to EP20789572.3A priority patent/EP4041720A1/en
Publication of WO2021069575A1 publication Critical patent/WO2021069575A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P5/00—Nematocides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P7/00—Arthropodicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to novel heteroaryl-substituted pyrazine derivatives, to formulations and compositions comprising such compounds and to their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.
  • Certain heteroaryl-triazole and heteroaryl-tetrazole compounds are disclosed for the use in controlling of ectoparasites on animals in WO 2017/192385 and for the use in controlling of animal pests in the field of plant protection in WO 2019/170626 and WO 2019/215198.
  • WO 2020/002563, WO 2020/053364, WO 2020/053365, WO 2020/079198 and WO 2020/169445 describe azole-amide compounds whereas WO 2020/070049 relates to pyrazine compounds all of which can be used as insecticides.
  • the invention relates to compounds of the general formula (I) in which R 1 is hydrogen; in each case optionally substituted C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 3 - C 6 cycloalkylC 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkynyl; or phenyl-C 1 -C 6 alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH 3 )3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C 6
  • R 41 is hydrogen or in each case optionally substituted C 1 -C 6 alkyl, C 1 - C 6 haloalkyl, C 3 -C 6 cycloalkyl, -C 1 -C 6 alkyl-C 3 -C 6 cycloalkyl, phenyl, heteroaryl and heterocyclyl;
  • R 42 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl and C3-C6cycloalkyl;
  • R 43 is independently selected from in each case optionally substituted C1- C6alkyl, C1-C6haloalkyl, C3-C6cycloalkyl and phenyl;
  • R 44 is in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C6haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and
  • the compounds of the formula (I) described anywhere herein likewise encompass any diastereomers or enantiomers and E/Z isomers which exist, and also salts and N-oxides of compounds of the formula (I).
  • the compounds of the formula (I) described anywhere herein may possibly also, depending on the nature of the substituents, be in the form of stereoisomers, i.e. in the form of geometric and/or optical isomers or isomer mixtures of varying composition. This invention provides both the pure stereoisomers and any desired mixtures of these isomers, even though it is generally only compounds of the formula (I) that are discussed here.
  • dextrorotatory compounds of formula (I) are preferred, i.e. those isomers which rotate plane-polarized light clockwise ((+)-direction).
  • Such enantiomers are usually designated with “(+)“.
  • the present cocompounds can have R- or S- configuration (according to the Cahn-Ingold-Prelog rules).
  • the present invention relates to compounds which have R- or S-configuration at this site as well as to mixtures of these isomers.
  • compounds of formula (I) are preferred which have an S-configuration at the carbon atom which carries R 3 .
  • the compounds of the formula (I) may be present in various polymorphic forms or as a mixture of various polymorphic forms. Both the pure polymorphs and the polymorph mixtures are provided by the invention and can be used in accordance with the invention.
  • R 4 is pyridine, pyrimidine, pyrazine or pyridazine wherein the pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, independently selected, from C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C3-C4cycloalkyl, halogen and hydroxy.
  • R 4 is pyridine or pyrimidine wherein the pyridine or pyrimidine is optionally substituted with one substituent selected from C1-C3alkyl, C3-C4cycloalkyl or halogen or hydroxy; or wherein preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from,C3-C4cycloalkyl or halogen and hydroxy; or wherein more preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from C3-C4cycloalkyl, F, Cl and Br.
  • the invention relates to compounds of the general formula (I) in which R 1 is hydrogen; in each case optionally substituted C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 3 - C 6 cycloalkylC 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 3 alkoxyC 1 -C 3 alkyl, C 1 - C 3 alkylthioC 1 -C 3 alkyl, C 1 -C 3 alkylsulfinylC 1 -C 3 alkyl, C 1 -C 3 alkylsulfonylC 1 -C 3 alkyl, C 1 - C 3 haloalkyl, C 1 -C 6 cyanoalkyl; or phenyl-C 1 -C 6 alkyl, in which phenyl is optionally substituted with 1 to 5 substituent
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; or in each case optionally substituted C 1 -C 6 alkyl, C 3 -C 6 cycloalkylC 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxyC 1 -C 6 alkyl, C 1 -C 6 alkylthioC 1 -C 6 alkyl, C 1 - C 6 alkylsulfinylC 1 -C 6 alkyl, C 1 -C 6 alkylsulfonylC 1 -C 6 alkyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH 3 )3, -NH2 and C1-C6al
  • the invention relates to compounds or the formula (I) as described supra, in which R 1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3haloalkyl, C1-C6cyanoalkyl; or phenyl-C 1 -C 6 alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH 2 , -CSNH 2 , -NO 2 , -Si(CH 3 ) 3 , -SF 5 , -NH 2 , C 1 -
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; or C 1 -C 6 alkyl, C 3 -C 6 cycloalkylC 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 - C 6 alkynyl, C 2 -C 6 haloalkynyl, C 1 -C 3 alkoxyC 1 -C 3 alkyl, C 1 -C 3 alkylthioC 1 -C 3 alkyl, C 1 - C 3 alkylsulfinylC 1 -C 3 alkyl, C 1 -C 3 alkylsulfonylC 1 -C 3 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 cyanoalkyl; R 2 is selected from the group consisting of pyrazole, phenyl,
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; or C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2- C6alkynyl, C2-C6haloalkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3alkylsulfinylC1-C3alkyl, C1-C3alkylsulfonylC1-C3alkyl, C1-C6haloalkyl, C1-C6cyanoalkyl; R 2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substitute
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C 6 cyanoalkyl;
  • R 2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH 2 , -NO 2 , -NH 2 , SF 5 , C 1 -C 6 alkyl, C 3 -C 6
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, methylsulfonylethyl, ethylsulfonylethyl; R 2 is selected from the group consisting of pyrazole, phenyl and pyridine each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, -SF5, methyl, ethyl, n-propyl, isopropyl,
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, methylsulfonylethyl, ethylsulfonylethyl; R 2 is selected from the group consisting of phenyl and pyridine each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl,
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl; R 2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl,
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen, or cyclopropylmethyl; R 2 is selected from the group consisting of pyrazol, phenyl and pyridine, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, tert- butyl, 1-cyano-1-methyleth-1-yl, cyclopropyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsul
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen, or cyclopropylmethyl; R 2 is selected from the group consisting of phenyl and pyridine, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, -CN, -SF 5 , methyl, ethyl, n-propyl, isopropyl, tert-butyl, cyclopropyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl; R 3 is methyl; R 4 is selected from the group consisting of pyridine-2-yl, pyrimidin-2-yl,
  • the invention relates to compounds of the formula (I) as described supra, in which R 1 is hydrogen, methyl, cyclopropylmethyl, ethoxymethyl or ethylthiomethyl; R 2 is selected from the group consisting of phenyl and pyridine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of fluorine, chlorine, bromine, CN, SF 5 , methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, trifluoromethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, isopropan-2-ol, (CH 3 ) 3 -silyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl
  • the invention relates to compounds of the formula (I) as described supra, in which R 2 is phenyl which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof.
  • R 25 and R 26 are preferably defined as follows:
  • R 25 is -SO2NH2, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH 3 )3-silyl, cyanomethoxy, tert-butyl, cyclopropyl, cyanomethyl, 1-cyano-1-methyleth-1-yl, 1-cyanocyclopropyl, isopropan-2-ol, phenylsulfonyl which may optionally carry a fluorine substituent; or is oxetane, tetrahydropyrane or piperazine which each may optionally carry a methyl substituent;
  • R 26 is fluorine, chlorine, bromine, CN, SF 5 , methyl, ethyl, n-propyl, isopropyl, buty
  • R 25 and R 26 are preferably defined as follows:
  • R 25 is -SO 2 NH 2 , methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, (CH 3 ) 3 -silyl, cyanomethoxy, tert-butyl, cyclopropyl, cyanomethyl, isopropan-2-ol, phenylsulfonyl which may optionally carry a fluorine substituent; or is oxetane, tetrahydropyrane or piperazine which each may optionally carry a methyl substituent;
  • R 26 is fluorine, chlorine, bromine, CN, SF 5 , methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluorometh
  • R 25 and R 26 are particularly preferably defined as follows: R 25 is methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, tert-butyl, cyclopropyl, 1-cyano-1-methyleth-1-yl,1-cyanocyclopropyl, 4-fluorophenylsulfonyl; and R 26 is fluorine, chlorine, bromine, iodine, CN, SF5, methyl, ethyl, isopropyl, tert.-butyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl.
  • R 25 and R 26 are particularly preferably defined as follows: R 25 is methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, tert-butyl, cyclopropyl; and R 26 is fluorine, chlorine, bromine, CN, SF5, methyl, ethyl, isopropyl, tert.-butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl.
  • R 27 and R 28 are preferably defined as follows: R 27 is fluorine, chlorine, bromine, -CN, -SF 5 , methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy; R 28 is fluorine, chlorine, bromine, -CN, -SF 5 , methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy.
  • the invention relates to compounds of the formula (I) as described supra, in which R 2 is thiophene, pyrazole or imidazole, each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof.
  • R 2 is selected from an optionally substituted thiophene and a pyrazole group: wherein R 9 is selected from halogen, preferably fluorine, chlorine and bromine, C 1 -C 3 alkyl, preferably methyl, C 1 - C 3 haloalkyl, preferably trifluoromethyl, and pentafluorosulfanyl; n is an integer of 0, 1 or 2, preferably 1 or 2; and Y represents hydrogen, C 1 -C 3 alkyl, preferably methyl and ethyl, cycloalkyl, preferably cyclopropyl, C 1 - C 3 haloalkyl, preferably trifluoromethyl.
  • R 9 is selected from halogen, preferably fluorine, chlorine and bromine, C 1 -C 3 alkyl, preferably methyl, C 1 - C 3 haloalkyl, preferably trifluoromethyl, and pentafluorosulfanyl
  • n is an integer of 0, 1 or
  • R 2 are represented by the following formulae: * * .
  • the invention relates to compounds of the formula (I) as described supra, in which R 4 is selected from the group consisting of pyridine, pyrimidine, thiazole, pyrazol and pyrazine each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof.
  • R 4 is selected from the group consisting of pyridine, pyrimidine and thiazole, each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N- oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-i), (I-ii) or (I-iii) wherein R 1 , R 2 , R 3 , R 5 and R 6 have the meaning as defined in any of the aspects described supra; and R 8 represents 0, 1, 2, 3 or 4 same or different substituents as defined in any of the aspects described anywhere supra for R 4 , preferably R 8 represents 0, 1 or 2 substituents, more preferably 0 or 1 substituents; and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-i) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH 3 (cyclopropylmethyl), CO-N-pyrrolidinyl, CON(CH 3 (CH 2 CN); and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-i) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of -CN, -COOH, -COOCH 3 , - COOCH 2 CH 3 , and the substructure S13, in which the bond marked with # is connected to the pyridine, preferably in C-5-position, and Z is CO;
  • R 41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl or cyclopropyl;
  • R 42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyan
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-ii) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH 3 (cyclopropylmethyl), CO-N-pyrrolidinyl, CON(CH 3 (CH 2 CN); and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-ii) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of -CN, -COOH, -COOCH 3 , - COOCH 2 CH 3 , and the substructure S13, in which the bond marked with # is connected to the pyrimidine, preferably in C-5-position, and Z is CO;
  • R 41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl, or cyclopropyl;
  • R 42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-iii) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH 3 (cyclopropylmethyl), CO- N-pyrrolidinyl, CON(CH 3 (CH 2 CN); and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-iii) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH 3 , - COOCH 2 CH 3 , and the substructure S13, in which the bond marked with # is connected to the thiazole, preferably to the C-5-position, and Z is CO; R 41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-iv) wherein R 1 , R 2 , R 3 , R 5 and R 6 have the meaning as defined in any of the aspects described supra; and R 8 represents 0, 1, 2 or 3 same or different substituents as defined in any of the aspects described anywhere supra for R 4 , preferably R 8 represents 0, 1 or 2 substituents, more preferably 0 or 1 substituents; and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-iv) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH 3 (cyclopropylmethyl), CO- N-pyrrolidinyl, CON(CH 3 (CH 2 CN); and salts and N-oxides thereof.
  • the compounds of the formula (I) are characterized by having a structure according to formula (I-iv) supra, and R 1 , R 2 , R 3 , R 5 , R 6 have the meaning as defined in any of the aspects described supra and R 8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH 3 , -COOCH 2 CH 3 , and the substructure S13, in which the bond marked with # is connected to the thiazole, preferably to the C-5-position, and Z is CO; R 41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n
  • the invention relates to compounds of the formula (I) as described in any of the aspects supra, which are characterized by having a structure according to formula (I-v), (I-vi) or (I- vii) in which R 1 , R 3 , R 5 and R 6 have the meaning as defined in any of the aspects described supra; R 7 represents same or different substituents of R 2 as defined in any of the aspects described supra; R 8 represents same or different substituents of R 4 as defined in any of the aspects described supra; n represents an integer of 0, 1 or 2, preferably 0 or 1; m represents an integer of 0, 1 or 2, preferably of 1 or 2; and salts and N-oxides thereof.
  • the invention is directed to compounds of formula (I-v) as defined above. According to a further preferred embodiment of the aspect 9 the invention is directed to compounds of formula (I-vi) as defined above. According to a preferred embodiment of the aspect 9 the invention is directed to compounds of formula (I-vii) as defined above. In a further aspect (aspect 10) the invention relates to compounds of the formula (I) as described in any of the aspects supra, which are characterized by having a structure according to one of the formulae (I-viii), (I-ix), (I-x), (I-xi) and (I-xii)
  • R 1 , R 3 , R 5 and R 6 have the meaning as defined in any of the aspects described supra;
  • R 7 represents same or different substituents of R 2 as defined in any of the aspects described supra;
  • R 8 represents same or different substituents of R 4 as defined in any of the aspects described supra;
  • n represents an integer of 0, 1 or 2, preferably 0 or 1;
  • m represents an integer of 0, 1 or 2, preferably of 1 or 2; and salts and N-oxides thereof.
  • the invention is directed to compounds of formula (I- viii) as defined above.
  • the invention is directed to compounds of formula (I-ix) as defined above.
  • the invention is directed to compounds of formula (I-x) as defined above.
  • the invention is directed to compounds of formula (I-xi) as defined above.
  • the aspect 10 of the invention relates to compounds of formulae (I- xii), (I-xiii), (I-xiv), (I-xv), (I-xvi), (I-xvii), (I-xviii) or (I-xix)
  • R 1 , R 3 , R 5 and R 6 have the meaning as defined in any of the aspects described supra;
  • R 7 represents same or different substituents of R 2 as defined in any of the aspects described supra;
  • R 8 represents same or different substituents of R 4 as defined in any of the aspects described supra;
  • the invention is directed to compounds of formula (I-xii) as defined above. According to a further preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xiii) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xiii) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xiv) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xv) as defined above. According to a further preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xvi) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xvii) as defined above.
  • the invention is directed to compounds of formula (I-xviii) as defined above.
  • the invention is directed to compounds of formula (I-xix) as defined above.
  • the invention is directed to compounds of formula (I) as described in the various aspects and embodiments herein, wherein R 5 represents hydrogen and the other substituents may have any of the meanings described herein.
  • the invention is directed to compounds of formula (I) as described in the various aspects and embodiments herein, wherein R 6 does not represent hydrogen and the other substituents may have any of the meanings described herein.
  • a further aspect (aspect 11) of the invention relates to the Intermediate Compounds according to formula IX-1, X or XIII wherein R 3 , R 4 , R 5 and R 6 have the meaning as defined in any of the aspects of the invention supra.
  • an alkyl group may consist of 3 to 10 carbon atoms and in that case corresponds to C3-C10alkyl.
  • Ring structures composed of carbon atoms and heteroatoms may be referred to as "LL- to UL-membered" structures.
  • One example of a 6-membered ring structure is toluene (a 6- membered ring structure substituted by a methyl group).
  • a collective term for a substituent for example CLL-CULalkyl
  • the constituent at the start of the composite substituent for example the CLL-CULcycloalkyl
  • the constituent at the start of the composite substituent for example the CLL-CULcycloalkyl
  • All the collective terms used in this application for chemical groups, cyclic systems and cyclic groups can be stipulated more specifically through the addition "CLL-CUL" or "LL- to UL-membered".
  • Halogen relates to elements of the 7th main group, preferably fluorine, chlorine, bromine and iodine, more preferably fluorine, chlorine and bromine, and even more preferably fluorine and chlorine.
  • heteroatom are N, O, S, P, B, Si.
  • heteroatom relates to N, S and O.
  • alkyl on its own or as part of a chemical group – represents straight-chain or branched hydrocarbons preferably having 1 to 6 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,2- dimethylpropyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2- methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,2-dimethylpropyl, 1,3-dimethylbutyl, 1,4- dimethylbutyl, 2,3-dimethylbutyl, 1,1-dimethylbutyl, 2,2-dimethylbutyl, 3,3-dimethyl
  • alkyls having 1 to 4 carbon atoms such as, inter alia, methyl, ethyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl or t-butyl.
  • inventive alkyls may be substituted by one or more identical or different radicals.
  • alkenyl on its own or as part of a chemical group – represents straight- chain or branched hydrocarbons preferably having 2 to 6 carbon atoms and at least one double bond, for example vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3- butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1- ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2- pentenyl, 3-methyl-2-pentenyl, for example vinyl,
  • alkenyls having 2 to 4 carbon atoms such as, inter alia, 2-propenyl, 2-butenyl or 1-methyl-2-propenyl.
  • inventive alkenyls may be substituted by one or more identical or different radicals.
  • alkynyl on its own or as part of a chemical group – represents straight- chain or branched hydrocarbons preferably having 2 to 6 carbon atoms and at least one triple bond, for example 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1- methyl-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2- propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1- methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyn
  • alkynyls having 2 to 4 carbon atoms such as, inter alia, ethynyl, 2-propynyl or 2-butynyl-2-propenyl.
  • inventive alkynyls may be substituted by one or more identical or different radicals.
  • cycloalkyl on its own or as part of a chemical group – represents mono-, bi- or tricyclic hydrocarbons preferably having 3 to 10 carbons, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, bicyclo[2.2.1]heptyl, bicyclo[2.2.2]octyl or adamantyl.
  • alkylcycloalkyl represents mono-, bi- or tricyclic alkylcycloalkyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example methylcyclopropyl, ethylcyclopropyl, isopropylcyclobutyl, 3-methylcyclopentyl and 4-methylcyclohexyl. Preference is also given to alkylcycloalkyls having 4, 5 or 7 carbon atoms such as, inter alia, ethylcyclopropyl or 4-methylcyclohexyl.
  • cycloalkylalkyl represents mono-, bi- or tricyclic cycloalkylalkyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl and cyclopentylethyl. Preference is also given to cycloalkylalkyls having 4, 5 or 7 carbon atoms such as, inter alia, cyclopropylmethyl or cyclobutylmethyl.
  • hydroxyalkyl represents a straight-chain or branched alcohol preferably having 1 to 6 carbon atoms, for example methanol, ethanol, n-propanol, isopropanol (isopropan-2-ol), n- butanol, isobutanol, s-butanol and t-butanol. Preference is also given to hydroxyalkyl groups having 1 to 4 carbon atoms.
  • the inventive hydroxyalkyl groups may be substituted by one or more identical or different radicals.
  • alkoxy represents a straight-chain or branched O-alkyl preferably having 1 to 6 carbon atoms, for example methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, s-butoxy and t-butoxy. Preference is also given to alkoxy groups having 1 to 4 carbon atoms. The inventive alkoxy groups may be substituted by one or more identical or different radicals.
  • cycloalkoxy represents a -O-cycloalkyl group, wherein cycloalkyl has the meaning as defined supra. Preference is given to cycloalkyls having 3, 4, 5, 6 or 7 carbon atoms, i.e.
  • inventive cycloalkoxy groups may be substituted by one or more identical or different radicals, preferably optional substituents are selected from halogens.
  • alkylthio represents straight-chain or branched S-alkyl preferably having 1 to 6 carbon atoms, for example methylthio, ethylthio, n-propylthio, isopropylthio, n- butylthio, isobutylthio, s-butylthio and t-butylthio. Preference is also given to alkylthio groups having 1 to 4 carbon atoms.
  • the inventive alkylthio groups may be substituted by one or more identical or different radicals.
  • alkylsulfinyl represents straight-chain or branched alkylsulfinyl preferably having 1 to 6 carbon atoms, for example methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, s-butylsulfinyl and t-butylsulfinyl. Preference is also given to alkylsulfinyl groups having 1 to 4 carbon atoms.
  • alkylsulfinyl groups may be substituted by one or more identical or different radicals.
  • alkylsulfonyl represents straight-chain or branched alkylsulfonyl preferably having 1 to 6 carbon atoms, for example methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, s-butylsulfonyl and t-butylsulfonyl.
  • alkylsulfonyl groups having 1 to 4 carbon atoms.
  • the inventive alkylsulfonyl groups may be substituted by one or more identical or different radicals.
  • cycloalkylsulfonyl represents mono-, bi- or tricyclic cycloalkylsulfonyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl and cyclohexylsulfonyl.
  • cycloalkylsulfonyls having 4, 5 or 7 carbon atoms such as, inter alia, cyclopropylsulfonyl or cyclobutylsulfonal.
  • the inventive cycloalkylsulfonyls may be substituted by one or more identical or different radicals.
  • alkylcarbonyls having 1 to 4 carbon atoms Preference is also given to alkylcarbonyls having 1 to 4 carbon atoms.
  • Alkylcarbonyls may be substituted by one or more identical or different radicals.
  • alkoxycarbonyl alone or as a constituent of a chemical group - represents straight-chain or branched alkoxycarbonyl, preferably having 1 to 6 carbon atoms or having 1 to 4 carbon atoms in the alkoxy moiety, for example methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, s-butoxycarbonyl and t-butoxycarbonyl.
  • Alkoxycarbonyl groups may be substituted by one or more identical or different radicals.
  • alkylaminocarbonyl represents straight-chain or branched alkylaminocarbonyl having preferably 1 to 6 carbon atoms or 1 to 4 carbon atoms in the alkyl moiety, for example methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl, s- butylaminocarbonyl and t-butylaminocarbonyl.
  • Alkylaminocarbonyl groups may be substituted by one or more identical or different radicals.
  • N,N-dialkylaminocarbonyl represents straight-chain or branched N,N- dialkylaminocarbonyl having preferably 1 to 6 carbon atoms or 1 to 4 carbon atoms in the alkyl moiety, for example N,N-dimethylaminocarbonyl, N,N-diethylaminocarbonyl, N,N-di(n-propylamino)carbonyl, N,N-di(isopropylamino)carbonyl and N,N-di-(s-butylamino)carbonyl.
  • N,N-dialkylaminocarbonyl groups may be substituted by one or more identical or different radicals.
  • aryl represents a mono-, bi- or polycyclic aromatic system having preferably 6 to 14, especially 6 to 10, ring carbon atoms, for example phenyl, naphthyl, anthryl, phenanthrenyl, preferably phenyl.
  • Aryl may also represent polycyclic systems, including fused polycyclic systems, such as tetrahydronaphthyl, indenyl, indanyl, fluorenyl, biphenyl, where the bonding site is on the aromatic system.
  • a fused polycyclic system has at least two fused rings, wherein these two fused rings share two adjacent atoms (or, iIn other words, the rings share one covalent bond). Preference is given to phenyl.
  • inventive aryl groups in particular phenyl groups, may be substituted by one or more identical or different radicals.
  • polycyclic refers to fused, bridged and spirocyclic carbocyclic and heterocyclic rings as well as ring systems linked through single or double bonds.
  • heterocycle represents a carbocyclic ring system having at least one ring in which at least one carbon atom is replaced by a heteroatom, preferably by a heteroatom from the group consisting of N, O, S, P, B, Si, Se, and which is saturated, unsaturated or heteroaromatic and may be unsubstituted or substituted, where the bonding site is on a ring atom.
  • the heterocyclic ring contains 3 to 12 ring atoms, preferably 3 to 9 ring atoms, especially 3 to 6 ring atoms, and one or more, preferably 1 to 4, especially 1, 2 or 3, heteroatoms in the heterocyclic ring, preferably from the group consisting of N, O, and S, although no two oxygen atoms should be directly adjacent.
  • the heterocyclic rings usually contain not more than 4 nitrogen atoms and/or not more than 2 oxygen atoms and/or not more than 2 sulphur atoms.
  • Non-aromatic heterocycles herein are usually referred to as “saturated or unsatured heterocycle”.
  • heterocyclyl radical or the heterocyclic ring When the heterocyclyl radical or the heterocyclic ring is optionally substituted, it may be fused to other carbocyclic or heterocyclic rings.
  • the invention also embraces polycyclic systems, for example 8-azabicyclo[3.2.1]octanyl, 1-azabicyclo[2.2.1]heptyl, 1-oxa-5- azaspiro[2.3]hexyl or 2,3-dihydro-1H-indole.
  • spirocyclic systems for example 1-oxa-5-azaspiro[2.3]hexyl.
  • Preferred heterocyclyl groups of the invention are, for example, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, dihydropyranyl, tetrahydropyranyl, dioxanyl, pyrrolinyl, pyrrolidinyl, imidazolinyl, imidazolidinyl, thiazolidinyl, oxazolidinyl, dioxolanyl, dioxolyl, pyrazolidinyl, tetrahydrofuranyl, dihydrofuranyl, oxetanyl, oxiranyl, azetidinyl, aziridinyl, oxazetidinyl, oxaziridinyl, oxazepanyl, oxazinanyl, azepanyl, oxopyrrolidinyl, dioxopyrrolidinyl, oxomorpholin
  • heteroaryl i.e. heteroaromatic systems.
  • heteroaryl represents heteroaromatic compounds, i.e. completely unsaturated aromatic heterocyclic compounds which fall under the above definition of heterocycles.
  • heterocycle or “heterocyclyl”
  • heteroaryl or “heteroaromatic”
  • heteroaryls are, for example, furyl, thienyl, pyrazolyl, imidazolyl, 1,2,3- and 1,2,4-triazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-, 1,3,4-, 1,2,4- and 1,2,5-oxadiazolyl, azepinyl, pyrrolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1,3,5-, 1,2,4- and 1,2,3-triazinyl, 1,2,4-, 1,3,2-, 1,3,6- and 1,2,6-oxazinyl, oxepinyl, thiepinyl, 1,2,4-triazolonyl and 1,2,4
  • pyridinyl Preference is given to pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrazolyl, pyrrolyl, thiazolyl, oxazolyl, isothiazolyl, and isoxazolyl. More preferred are pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrazolyl, pyrrolyl, and thiazolyl.
  • the inventive heteroaryl groups may also be substituted by one or more identical or different radicals.
  • each case optionally substituted means that a group/substituent , such as a alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cycloalkyl, aryl, phenyl, benzyl, heterocyclyl and heteroaryl radical etc., may be substituted, meaning, for example, a substituted radical derived from the unsubstituted base structure, where the substituents, for example, one (1) substituent or a plurality of substituents, preferably 1, 2, 3, 4, 5, 6 or 7, more preferably 1, 2, 3 or 4 substituents, more preferably 1, 2 or 3 substituents, even more preferred 1 or 2 substituents, are independently selected from a group consisting of amino, hydroxyl, halogen, nitro, cyano, isocyano, mercapto, isothiocyanato, C1-C4carboxyl,
  • first substituent level may, if they contain hydrocarbonaceous components, optionally have further substitution therein (“second substituent level”), for example by one or more of the substituents each independently selected from halogen, hydroxyl, C 1 -C 6 alkyl, amino, nitro, cyano, isocyano, azido, acylamino, an oxo group and an imino group.
  • halogen-substituted chemical groups or halogenated groups are mono- or polysubstituted by halogen up to the maximum possible number of substituents.
  • Such groups are also referred to as halo groups (for example haloalkyl, halocycloalkyl, haloalkoxy, haloalkylthio, haloalkylsulfinyl, or haloalkylsulfonyl etc.).
  • the halogen atoms may be the same or different, and may all be bonded to one carbon atom or may be bonded to a plurality of carbon atoms.
  • Halogen is especially fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine and more preferably fluorine or chlorine, even more preferred is fluorine.
  • halogen-substituted groups are monohalocycloalkyl such as 1-fluorocyclopropyl, 2-fluorocyclopropyl or 1-fluorocyclobutyl, monohaloalkyl such as 2-chloroethyl, 2-fluoroethyl, 1-chloroethyl, 1-fluoroethyl, chloromethyl, or fluoromethyl; perhaloalkyl such as trichloromethyl or trifluoromethyl or CF2CF3, polyhaloalkyl such as difluoromethyl, 2-fluoro-2-chloroethyl, dichloromethyl, 1,1,2,2-tetrafluoroethyl or 2,2,2-trifluoroethyl.
  • monohaloalkyl such as 2-chloroethyl, 2-fluoroethyl, 1-chloroethyl, 1-fluoroethyl, chloromethyl, or fluoromethyl
  • perhaloalkyl
  • haloalkyls are trichloromethyl, chlorodifluoromethyl, dichlorofluoromethyl, chloromethyl, bromomethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2,2,2- trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 3,3,3-trifluoropropyl and pentafluoro-t-butyl.
  • haloalkyls having 1 to 4 carbon atoms and 1 to 9, preferably 1 to 5, identical or different halogen atoms selected from fluorine, chlorine and bromine. Particular preference is given to haloalkyls having 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms selected from fluorine and chlorine, such as, inter alia, difluoromethyl, trifluoromethyl or 2,2-difluoroethyl.
  • halogen-substituted compounds are haloalkoxy such as OCF3, OCHF2, OCH 2 F, OCF2CF3, OCH 2 CF3, OCH 2 CHF2 und OCH 2 CH 2 Cl; haloalkylsulfanyls such as difluoromethylthio, trifluoromethylthio, trichloromethylthio, chlorodifluoromethylthio, 1-fluoroethylthio, 2-fluoroethylthio, 2,2-difluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2,2,2-trifluoroethylthio or 2-chloro-1,1,2-trifluoroethylthio; haloalkylsulfinyls such as difluoromethylsulfinyl, trifluoromethylsulfinyl, trichloromethylsulfinyl, chlorodifluoromethylmethyl
  • the inventive cyano-substituted chemical groups are preferably monosubstituted by cyano.
  • Such cyano-substituted groups are also referred to as cyano groups (for example cyanoalkyl, cyanocycloalkyl, cyanoalkoxy, cyanoalkylthio, cyanoalkylsulfinyl, cyanoalkylsufonyl etc.).
  • C LL - UL cyanoalkyl If the number of carbon atoms is specified in such cyano groups, for example C LL - UL cyanoalkyl, the carbon atom of the cyano group will not be counted; e.g. C 1-3 cyanoalkyl includes cyanopropyl groups.
  • radicals having carbon atoms preference is given to those having 1 to 4 carbon atoms, especially 1 or 2 carbon atoms.
  • substituents from the group of halogen e.g.
  • Substituted amino such as mono- or disubstituted amino means a radical from the group of the substituted amino radicals which are N-substituted, for example, by one or two identical or different radicals from the group of alkyl, hydroxy, amino, alkoxy, acyl and aryl; preferably N-mono- and N,N-dialkylamino, (for example methylamino, ethylamino, N,N-dimethylamino, N,N-diethylamino, N,N-di-n-propylamino, N,N- diisopropylamino or N,N-dibutylamino), N-mono- or N,N-dialkoxyalkylamino groups (for example N- methoxymethylamino, N-methoxyethylamino, N,N-di(methoxymethyl)amino or N,N- di(methoxyethyl)amino),
  • Substituted amino also includes quaternary ammonium compounds (salts) having four organic substituents on the nitrogen atom.
  • Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals from the group of halogen, SF5, (C1- C4)alkyl, C3-C6cycloalkyl, (C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkyl, (C1-C4)haloalkyl, (C1-C4)haloalkoxy, hydroxy-C1-C4alkyl, (C1-C4)alkylthio, (C1-C4)haloalkylthio, (C1- C4)alkyl
  • Optionally substituted cycloalkyl is preferably cycloalkyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals from the group of halogen, cyano, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, (C 1 -C 4 )alkoxy-(C 1 -C 4 )alkoxy, (C 1 -C 4 )alkoxy-(C 1 -C 4 )alkyl, (C 1 - C 4 )haloalkyl and (C 1 -C 4 )haloalkoxy, especially by one or two (C 1 -C 4 )alkyl radicals.
  • Inventive compounds may occur in preferred embodiments. Individual embodiments described herein may be combined with one another. Not included are combinations which contravene the laws of nature and which the person skilled in the art would therefore rule out on the basis of his/her expert knowledge. Ring structures having three or more adjacent oxygen atoms, for example, are excluded. Isomers Depending on the nature of the substituents, the compounds of the formula (I) may be in the form of geometric and/or optically active isomers or corresponding isomer mixtures in different compositions. These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers. Accordingly, the invention encompasses both pure stereoisomers and any mixture of these isomers.
  • the invention also relates to methods for controlling animal pests, in which compounds of the formula (I) are allowed to act on animal pests and/or their habitat.
  • the control of the animal pests is preferably conducted in agriculture and forestry, and in material protection.
  • Preferably excluded herefrom are methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods carried out on the human or animal body.
  • the invention furthermore relates to the use of the compounds of the formula (I) as pesticides, in particular crop protection agents.
  • the term "pesticide” in each case also always comprises the term "crop protection agent".
  • the compounds of the formula (I), having good plant tolerance, favourable homeotherm toxicity and good environmental compatibility, are suitable for protecting plants and plant organs against biotic and abiotic stressors, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, especially insects, arachnids, helminths, in particular nematodes, and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in aquatic cultures, in forests, in gardens and leisure facilities, in the protection of stored products and of materials, and in the hygiene sector.
  • the term “hygiene” is understood to mean any and all measures, procedures and practices which aim to prevent disease, in particular infectious disease, and which serve to protect the health of humans and animals and/or to protect the environment, and/or which maintain cleanliness.
  • this especially includes measures for cleaning, disinfection and sterilisation of, for example, textiles or hard surfaces, especially surfaces of glass, wood, concrete, porcelain, ceramics, plastic or also of metal(s), and for ensuring that these are kept free of hygiene pests and/or their excretions.
  • surgical or therapeutic treatment procedures applicable to the human body or to the bodies of animals and diagnostic procedures which are carried out on the human body or on the bodies of animals.
  • honeygiene sector thus covers all areas, technical fields and industrial applications in which these hygiene measures, procedures and practices are important, in relation for example to hygiene in kitchens, bakeries, airports, bathrooms, swimming pools, department stores, hotels, hospitals, stables, animal husbandries, etc.
  • the term “hygiene pest” is therefore understood to mean one or more animal pests whose presence in the hygiene sector is problematic, in particular for health reasons. It is therefore a primary objective to avoid or minimize the presence of hygiene pests, and/or exposure to them, in the hygiene sector. This can be achieved in particular through the application of a pesticide that can be used both to prevent infestation and to tackle an infestation which is already present. Preparations which avoid or reduce exposure to pests can also be used.
  • Hygiene pests include, for example, the organisms mentioned below.
  • the term “hygiene protection” thus covers all actions to maintain and/or improve these hygiene measures, procedures and practices.
  • the compounds of the formula (I) can preferably be used as pesticides. They are active against normally sensitive and resistant species and against all or some stages of development.
  • pests from the phylum of the Arthropoda in particular from the class of the Arachnida, for example Acarus spp., for example Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., for example Aculus fockeui, Aculus Mattendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., for example Brevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus
  • Nephotettix spp. Myzus nicotianae, Nasonovia ribisnigri, Neomaskellia spp., Nephotettix spp., for example Nephotettix cincticeps,, Nephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., for example Paratrioza cockerelli, Parlatoria spp., Pemphigus spp., for example Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccus spp., for example Phenacoccus madeirensis, Phloeomy
  • phytoparasitic nematodes in particular Aglenchus spp., for example Aglenchus agricola, Anguina spp., for example Anguina tritici, Aphelenchoides spp., for example Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., for example Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp., for example Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., for example Cacopaurus pestis, Criconemella spp., for example Criconemella curvata, Criconemella onoensis, Criconemella ornata, Criconemella rusium, Criconemella
  • the compounds of the formula (I) can optionally, at certain concentrations or application rates, also be used as herbicides, safeners, growth regulators or agents to improve plant properties, as microbicides or gametocides, for example as fungicides, antimycotics, bactericides, viricides (including agents against viroids) or as agents against MLO (mycoplasma-like organisms) and RLO (rickettsia-like organisms). If appropriate, they can also be used as intermediates or precursors for the synthesis of other active compounds.
  • Formulations The present invention further relates to formulations, compositions and use forms comprising at least one compound of the formula (I) as defined anywhere supra.
  • Such formulations and compositions are in particular prepared as pesticides, for example drench, drip and spray liquors, comprising at least one compound of the formula (I).
  • Such formulations may further comprise at least one further compound selected from auxiliaries, excipients, solvents and/or additional pharmaceutically active agents.
  • the formulations or use forms comprise further pesticides and/or adjuvants which improve action, such as penetrants, e.g.
  • vegetable oils for example rapeseed oil, sunflower oil, mineral oils, for example paraffin oils, alkyl esters of vegetable fatty acids, for example rapeseed oil methyl ester or soya oil methyl ester, or alkanol alkoxylates and/or spreaders, for example alkylsiloxanes and/or salts, for example organic or inorganic ammonium or phosphonium salts, for example ammonium sulphate or diammonium hydrogenphosphate and/or retention promoters, for example dioctyl sulphosuccinate or hydroxypropyl guar polymers and/or humectants, for example glycerol and/or fertilizers, for example ammonium-, potassium- or phosphorus-containing fertilizers.
  • alkylsiloxanes and/or salts for example organic or inorganic ammonium or phosphonium salts, for example ammonium sulphate or diammonium hydrogenphosphate and/or retention promoter
  • Customary formulations are, for example, water-soluble liquids (SL), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS); these and further possible formulation types are described, for example, by Crop Life International and in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers – 173, prepared by the FAO/WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576.
  • auxiliaries for example extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, biocides, thickeners and/or further auxiliaries, for example adjuvants.
  • An adjuvant in this context is a component which enhances the biological effect of the formulation, without the component itself having any biological effect.
  • adjuvants are agents which promote retention, spreading, attachment to the leaf surface or penetration.
  • These formulations are prepared in a known way, for example by mixing the compounds of the formula (I) with auxiliaries such as, for example, extenders, solvents and/or solid carriers and/or other auxiliaries such as, for example, surfactants.
  • the formulations are prepared either in suitable facilities or else before or during application.
  • the auxiliaries used may be substances suitable for imparting special properties, such as certain physical, technical and/or biological properties, to the formulation of the compounds of the formula (I), or to the use forms prepared from these formulations (for example ready-to-use pesticides such as spray liquors or seed dressing products).
  • Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), the esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide), the carbonates and the nitriles.
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzen
  • suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example mineral oil fractions, mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide or dimethyl sulphoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, or nitriles such as acetonitrile or propanen
  • suitable solvents are aromatic hydrocarbons, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons, such as chlorobenzene, chloroethylene or methylene chloride, aliphatic hydrocarbons, such as cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols, such as methanol, ethanol, isopropanol, butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethyl sulphoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, nitriles such as acetonitrile or propanenitrile, and also water.
  • aromatic hydrocarbons such as xylene, tol
  • Useful carriers include especially: for example ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic materials such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and/or solid fertilizers. Mixtures of such carriers can likewise be used.
  • Useful carriers for granules include: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite, and synthetic granules of inorganic and organic meals, and also granules of organic material such as sawdust, paper, coconut shells, corn cobs and tobacco stalks.
  • Liquefied gaseous extenders or solvents can also be used.
  • Particularly suitable extenders or carriers are those which are gaseous at ambient temperature and under atmospheric pressure, for example aerosol propellant gases, such as halohydrocarbons, and also butane, propane, nitrogen and carbon dioxide.
  • emulsifiers and/or foam-formers, dispersants or wetting agents with ionic or nonionic properties, or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyl taurates), isethionate derivatives, phosphoric esters of polyethoxylated alcohols or phenols, fatty esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates,
  • a surfactant is advantageous if one of the compounds of the formula (I) and/or one of the inert carriers is insoluble in water and when the application takes place in water.
  • colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyes such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and nutrients and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc as further auxiliaries in the formulations and the use forms derived therefrom.
  • Additional components may be stabilizers, such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability. Foam formers or antifoams may also be present.
  • Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, or else natural phospholipids such as cephalins and lecithins and synthetic phospholipids may also be present as additional auxiliaries in the formulations and the use forms derived therefrom. Further possible auxiliaries are mineral and vegetable oils. Optionally, further auxiliaries may be present in the formulations and the use forms derived therefrom.
  • additives examples include fragrances, protective colloids, binders, adhesives, thickeners, thixotropic agents, penetrants, retention promoters, stabilizers, sequestrants, complexing agents, humectants, spreaders.
  • Useful retention promoters include all those substances which reduce the dynamic surface tension, for example dioctyl sulphosuccinate, or increase the viscoelasticity, for example hydroxypropylguar polymers.
  • Suitable penetrants in the present context are all those substances which are usually used for improving the penetration of agrochemical active compounds into plants.
  • Penetrants are defined in this context by their ability to penetrate from the (generally aqueous) application liquor and/or from the spray coating into the cuticle of the plant and thereby increase the mobility of active compounds in the cuticle.
  • the method described in the literature can be used to determine this property.
  • Examples include alcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters, for example rapeseed oil methyl ester or soya oil methyl ester, fatty amine alkoxylates, for example tallowamine ethoxylate (15), or ammonium and/or phosphonium salts, for example ammonium sulphate or diammonium hydrogenphosphate.
  • alcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecyl ethoxylate (12)
  • fatty acid esters for example rapeseed oil methyl ester or soya oil methyl ester
  • fatty amine alkoxylates for example tallowamine ethoxylate (15)
  • ammonium and/or phosphonium salts for example ammonium sulphate or diammonium hydrogenphosphate.
  • the formulations preferably comprise between 0.00000001 and 98% by weight of the compound of the formula (I) or, with particular preference, between 0.01% and 95% by weight of the compound of the formula (I), more preferably between 0.5% and 90% by weight of the compound of the formula (I), based on the weight of the formulation.
  • the content of the compound of the formula (I) in the use forms prepared from the formulations (in particular pesticides) may vary within wide ranges.
  • the concentration of the compound of the formula (I) in the use forms is usually between 0.00000001 and 95% by weight of the compound of the formula (I), preferably between 0.00001 and 1% by weight, based on the weight of the use form.
  • the compounds are employed in a customary manner appropriate for the use forms.
  • the compounds of the formula (I) may also be employed as a mixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficial species, herbicides, fertilizers, bird repellents, phytotonics, sterilants, safeners, semiochemicals and/or plant growth regulators, in order thus, for example, to broaden the spectrum of action, to prolong the duration of action, to increase the rate of action, to prevent repulsion or prevent evolution of resistance.
  • active compound combinations may improve plant growth and/or tolerance to abiotic factors, for example high or low temperatures, to drought or to elevated water content or soil salinity.
  • the compounds of the formula (I) can be present in a mixture with other active compounds or semiochemicals such as attractants and/or bird repellants and/or plant activators and/or growth regulators and/or fertilizers.
  • the compounds of the formula (I) can be used to improve plant properties such as, for example, growth, yield and quality of the harvested material.
  • the compounds of the formula (I) are present in formulations or the use forms prepared from these formulations in a mixture with further compounds, preferably those as described below. If one of the compounds mentioned below can occur in different tautomeric forms, these forms are also included even if not explicitly mentioned in each case. Further, all named mixing partners can, if their functional groups enable this, optionally form salts with suitable bases or acids. Insecticides/acaricides/nematicides
  • the active compounds identified here by their common names are known and are described, for example, in the pesticide handbook (“The Pesticide Manual” 16th Ed., British Crop Protection Council 2012) or can be found on the Internet (e.g. http://www.alanwood.net/pesticides).
  • Acetylcholinesterase (AChE) inhibitors preferably carbamates selected from alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb, or organophosphates selected from acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxy
  • GABA-gated chloride channel blockers preferably cyclodiene-organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fiproles) selected from ethiprole and fipronil.
  • Sodium channel modulators preferably pyrethroids selected from acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin s-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin,
  • Nicotinic acetylcholine receptor (nAChR) competitive modulators preferably neonicotinoids selected from acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam, or nicotine, or sulfoximines selected from sulfoxaflor, or butenolids selected from flupyradifurone, or mesoionics selected from triflumezopyrim.
  • Nicotinic acetylcholine receptor (nAChR) allosteric modulators preferably spinosyns selected from spinetoram and spinosad.
  • Glutamate-gated chloride channel (GluCl) allosteric modulators preferably avermectins/milbemycins selected from abamectin, emamectin benzoate, lepimectin and milbemectin.
  • Juvenile hormone mimics preferably juvenile hormone analogues selected from hydroprene, kinoprene and methoprene, or fenoxycarb or pyriproxyfen.
  • Miscellaneous non-specific (multi-site) inhibitors preferably alkyl halides selected from methyl bromide and other alkyl halides, or chloropicrine or sulphuryl fluoride or borax or tartar emetic or methyl isocyanate generators selected from diazomet and metam.
  • Chordotonal organ TRPV channel modulators selected from pymetrozine and pyrifluquinazone.
  • Mite growth inhibitors selected from clofentezine, hexythiazox, diflovidazin and etoxazole.
  • Microbial disruptors of the insect gut membrane selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis, and B.t. plant proteins selected from Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb and Cry34Ab1/35Ab1.
  • Inhibitors of mitochondrial ATP synthase preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotin, cyhexatin and fenbutatin oxide, or propargite or tetradifon.
  • Uncouplers of oxidative phosphorylation via disruption of the proton gradient selected from chlorfenapyr, DNOC and sulfluramid.
  • Nicotinic acetylcholine receptor channel blockers selected from bensultap, cartap hydrochloride, thiocylam and thiosultap-sodium.
  • Inhibitors of chitin biosynthesis type 0, selected from bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
  • Inhibitors of chitin biosynthesis type 1 selected from buprofezin.
  • Moulting disruptor in particular for Diptera, i.e. dipterans selected from cyromazine.
  • Ecdysone receptor agonists selected from chromafenozide, halofenozide, methoxyfenozide and tebufenozide.
  • Octopamine receptor agonists selected from amitraz.
  • Mitochondrial complex III electron transport inhibitors selected from hydramethylnone, acequinocyl and fluacrypyrim.
  • Mitochondrial complex I electron transport inhibitors preferably METI acaricides selected from fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad and tolfenpyrad, or rotenone (Derris).
  • Voltage-dependent sodium channel blockers selected from indoxacarb and metaflumizone.
  • Mitochondrial complex IV electron transport inhibitors preferably phosphines selected from aluminium phosphide, calcium phosphide, phosphine and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide and sodium cyanide.
  • Mitochondrial complex II electron transport inhibitors preferably beta-ketonitrile derivatives selected from cyenopyrafen and cyflumetofen, and carboxanilides selected from pyflubumide.
  • Mitochondrial complex II electron transport inhibitors preferably beta-ketonitrile derivatives selected from cyenopyrafen and cyflumetofen, and carboxanilides selected from pyflubumide.
  • Ryanodine receptor modulators preferably diamides selected from chlorantraniliprole, cyantraniliprole and flubendiamide.
  • Chordotonal organ Modulators (with undefined target site) selected from flonicamid.
  • Fungicides The active ingredients specified herein by their Common Name are known and described, for example, in The Pesticide Manual (16th Ed.British Crop Protection Council) or can be searched in the internet (e.g. www.alanwood.net/pesticides). All named fungicidal mixing partners of the classes (1) to (15) can, if their functional groups enable this, optionally form salts with suitable bases or acids. All named mixing partners of the classes (1) to (15) can include tautomeric forms, where applicable.
  • Inhibitors of the ergosterol biosynthesis for example (1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalil, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013) metconazole, (1.014) myclobutanil, (1.015) paclobutrazol, (1.016) prochloraz, (1.017) propiconazole, (1.018) prothioconazole, (1.019) Pyrisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022) tetraconazole, (1.023) t
  • Inhibitors of the respiratory chain at complex I or II for example (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad, (2.008) furametpyr, (2.009) Isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S
  • Inhibitors of the respiratory chain at complex III for example (3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxystrobin, (3.004) coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamid, (3.007) dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010) fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E)-2- ⁇ 2-[( ⁇ [(1E)-1-(3- ⁇ [(E)
  • Inhibitors of the mitosis and cell division for example (4.001) carbendazim, (4.002) diethofencarb, (4.003) ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate- methyl, (4.008) zoxamide, (4.009) 3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine, (4.010) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, (4.011) 3-chloro-5-(6- chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine, (4.012) 4-(2-bromo-4-fluorophenyl)- N-(2,6-difluorophenyl)-
  • Compounds capable to induce a host defence for example (6.001) acibenzolar-S-methyl, (6.002) isotianil, (6.003) probenazole, (6.004) tiadinil.
  • Inhibitors of the amino acid and/or protein biosynthesis for example (7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycin hydrochloride hydrate, (7.004) oxytetracycline, (7.005) pyrimethanil, (7.006) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline.
  • Inhibitors of the ATP production for example (8.001) silthiofam.
  • Inhibitors of the cell wall synthesis for example (9.001) benthiavalicarb, (9.002) dimethomorph, (9.003) flumorph, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) pyrimorph, (9.007) valifenalate, (9.008) (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (9.009) (2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one.
  • Inhibitors of the lipid and membrane synthesis for example (10.001) propamocarb, (10.002) propamocarb hydrochloride, (10.003) tolclofos-methyl.
  • Inhibitors of the melanin biosynthesis for example (11.001) tricyclazole, (11.002) 2,2,2-trifluoroethyl ⁇ 3-methyl-1-[(4-methylbenzoyl)amino]butan-2-yl ⁇ carbamate.
  • Inhibitors of the nucleic acid synthesis for example (12.001) benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam).
  • 13) Inhibitors of the signal transduction for example (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazid, (13.005) quinoxyfen, (13.006) vinclozolin.
  • Compounds capable to act as an uncoupler for example (14.001) fluazinam, (14.002) meptyldinocap.
  • Bio pesticides as mixing components
  • the compounds of the formula (I) can be combined with biological pesticides.
  • Biological pesticides comprise in particular bacteria, fungi, yeasts, plant extracts and products formed by microorganisms, including proteins and secondary metabolites.
  • Biological pesticides comprise bacteria such as spore-forming bacteria, root-colonising bacteria and bacteria which act as biological insecticides, fungicides or nematicides. Examples of such bacteria which are employed or can be used as biological pesticides are: Bacillus amyloliquefaciens, strain FZB42 (DSM 231179), or Bacillus cereus, in particular B.
  • thuringiensis subspecies israelensis (serotype H- 14), strain AM65-52 (Accession No. ATCC 1276), or B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), or B. thuringiensis subsp. kurstaki strain HD-1, or B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp.
  • fungi and yeasts which are employed or can be used as biological pesticides are: Beauveria bassiana, in particular strain ATCC 74040, Coniothyrium minitans, in particular strain CON/M/91-8 (Accession No.
  • Lecanicillium spp. in particular strain HRO LEC 12, Lecanicillium lecanii, (formerly known as Verticillium lecanii), in particular strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884/ ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (now: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No. ATCC 20874), Paecilomyces lilacinus, in particular P.
  • viruses which are employed or can be used as biological pesticides are: Adoxophyes orana (summer fruit tortrix) granulosis virus (GV), Cydia pomonella (codling moth) granulosis virus (GV), Helicoverpa armigera (cotton bollworm) nuclear polyhedrosis virus (NPV), Spodoptera exigua (beet armyworm) mNPV, Spodoptera frugiperda (fall armyworm) mNPV, Spodoptera littoralis (African cotton leafworm) NPV.
  • Adoxophyes orana sumr fruit tortrix granulosis virus
  • GV Cydia pomonella (codling moth) granulosis virus
  • NPV Helicoverpa armigera (cotton bollworm) nuclear polyhedrosis virus
  • Spodoptera exigua beet armyworm
  • Spodoptera frugiperda fall armyworm
  • bacteria and fungi which are added as 'inoculant' to plants or plant parts or plant organs and which, by virtue of their particular properties, promote plant growth and plant health.
  • Agrobacterium spp. Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., in particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., or Gigaspora monosporum, Glomus spp., Laccaria spp., Lactobacillus buchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp., Rhizobium spp., in particular Rhizobium trifolii, Rhizopogon spp., Scleroderma spp.
  • plant extracts and products formed by microorganisms including proteins and secondary metabolites which are employed or can be used as biological pesticides are: Allium sativum, Artemisia absinthium, azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodium anthelminticum, chitin, Armour-Zen, Dryopteris filix-mas, Equisetum arvense, Fortune Aza, Fungastop, Heads Up (Chenopodium quinoa saponin extract), Pyrethrum/Pyrethrins, Quassia amara, Quercus, Quillaja, Regalia, "Requiem TM Insecticide", rotenone, ryania/ryanodine, Symphytum officinale, Tanacetum vulgare, thymol, Triact 70, TriCon, Tropaeulum majus, Urtica dioica, Veratrin, Viscum album
  • Safener as mixing components can be combined with safeners such as, for example, benoxacor, cloquintocet (-mexyl), cyometrinil, cyprosulfamide, dichlormid, fenchlorazole (-ethyl), fenclorim, flurazole, fluxofenim, furilazole, isoxadifen (-ethyl), mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil, 2-methoxy-N-( ⁇ 4-[(methylcarbamoyl)amino]phenyl ⁇ sulphonyl)benzamide (CAS 129531- 12-0), 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (CAS 71526-07-3), 2,2,5-trimethyl-3- (dichloroacetyl)-1,3-oxazolidine (CAS 52), acoxib,
  • plants and plant parts can be treated in accordance with the invention.
  • plants are to be understood to mean all plants and plant parts such as wanted and unwanted wild plants or crop plants (including naturally occurring crop plants), for example cereals (wheat, rice, triticale, barley, rye, oats), maize, soya bean, potato, sugar beet, sugar cane, tomatoes, pepper, cucumber, melon, carrot, watermelon, onion, lettuce, spinach, leek, beans, Brassica oleracea (e.g. cabbage) and other vegetable species, cotton, tobacco, oilseed rape, and also fruit plants (with the fruits apples, pears, citrus fruits and grapevines).
  • cereals wheat, rice, triticale, barley, rye, oats
  • soya bean potato
  • sugar beet sugar cane
  • tomatoes pepper, cucumber, melon, carrot
  • watermelon onion
  • lettuce spinach
  • leek beans
  • Brassica oleracea e.g. cabbage
  • Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or cannot be protected by varietal property rights.
  • Plants should be understood to mean all developmental stages, such as seeds, seedlings, young (immature) plants up to mature plants.
  • Plant parts should be understood to mean all parts and organs of the plants above and below ground, such as shoot, leaf, flower and root, examples given being leaves, needles, stalks, stems, flowers, fruit bodies, fruits and seeds, and also tubers, roots and rhizomes.
  • Parts of plants also include harvested plants or harvested plant parts and vegetative and generative propagation material, for example seedlings, tubers, rhizomes, cuttings and seeds.
  • Treatment according to the invention of the plants and plant parts with the compounds of the formula (I) is carried out directly or by allowing the compounds to act on the surroundings, environment or storage space by the customary treatment methods, for example by immersion, spraying, evaporation, fogging, scattering, painting on, injection and, in the case of propagation material, in particular in the case of seeds, also by applying one or more coats.
  • wild plant species and plant cultivars or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and also parts thereof, are treated.
  • transgenic plants and plant cultivars obtained by genetic engineering methods if appropriate in combination with conventional methods (genetically modified organisms), and parts thereof are treated.
  • the term “parts” or “parts of plants” or “plant parts” has been explained above. The invention is used with particular preference to treat plants of the respective commercially customary cultivars or those that are in use. Plant cultivars are to be understood as meaning plants having new properties ("traits") and which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques.
  • transgenic plants or plant cultivars which are to be treated with preference in accordance with the invention include all plants which, through the genetic modification, received genetic material which imparts particular advantageous useful properties ("traits") to these plants. Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to levels of water or soil salinity, enhanced flowering performance, easier harvesting, accelerated ripening, higher yields, higher quality and/or a higher nutritional value of the harvested products, better storage life and/or processability of the harvested products.
  • Such properties are increased resistance of the plants against animal and microbial pests, such as against insects, arachnids, nematodes, mites, slugs and snails owing, for example, to toxins formed in the plants, in particular those formed in the plants by the genetic material from Bacillus thuringiensis (for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CryIF and also combinations thereof), furthermore increased resistance of the plants against phytopathogenic fungi, bacteria and/or viruses owing, for example, to systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and also resistance genes and correspondingly expressed proteins and toxins, and also increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulphonylureas, glyph
  • transgenic plants which may be mentioned are the important crop plants, such as cereals (wheat, rice, triticale, barley, rye, oats), maize, soya beans, potatoes, sugar beet, sugar cane, tomatoes, peas and other types of vegetable, cotton, tobacco, oilseed rape and also fruit plants (with the fruits apples, pears, citrus fruits and grapes), with particular emphasis being given to maize, soya beans, wheat, rice, potatoes, cotton, sugar cane, tobacco and oilseed rape.
  • Crop protection – types of treatment The treatment of the plants and plant parts with the compounds of the formula (I) is carried out directly or by action on their surroundings, habitat or storage space using customary treatment methods, for example by dipping, spraying, atomizing, irrigating, evaporating, dusting, fogging, broadcasting, foaming, painting, spreading-on, injecting, watering (drenching), drip irrigating and, in the case of propagation material, in particular in the case of seed, furthermore as a powder for dry seed treatment, a solution for liquid seed treatment, a water-soluble powder for slurry treatment, by incrusting, by coating with one or more coats, etc.
  • the compounds of the formula (I) by the ultra-low volume method or to inject the application form or the compound of the formula (I) itself into the soil.
  • a preferred direct treatment of the plants is foliar application, i.e. the compounds of the formula (I) are applied to the foliage, where treatment frequency and the application rate should be adjusted according to the level of infestation with the pest in question.
  • the compounds of the formula (I) also access the plants via the root system.
  • the plants are then treated by the action of the compounds of the formula (I) on the habitat of the plant. This may be done, for example, by drenching, or by mixing into the soil or the nutrient solution, i.e. the locus of the plant (e.g.
  • soil or hydroponic systems is impregnated with a liquid form of the compounds of the formula (I), or by soil application, i.e. the compounds of the formula (I) according to the invention are introduced in solid form (e.g. in the form of granules) into the locus of the plants, or by drip application (often also referred to as "chemigation"), i.e. the liquid application of the compounds of the formula (I) according to the invention from surface or sub-surface driplines over a certain period of time together with varying amounts of water at defined locations in the vicinity of the plants.
  • soil application i.e. the compounds of the formula (I) according to the invention are introduced in solid form (e.g. in the form of granules) into the locus of the plants, or by drip application (often also referred to as "chemigation"), i.e. the liquid application of the compounds of the formula (I) according to the invention from surface or sub-surface driplines over a certain period of time together with varying amounts
  • Treatment of seed The control of animal pests by treating the seed of plants has been known for a long time and is the subject of continuous improvements. However, the treatment of seed entails a series of problems which cannot always be solved in a satisfactory manner. Thus, it is desirable to develop methods for protecting the seed and the germinating plant which dispense with, or at least reduce considerably, the additional application of pesticides during storage, after sowing or after emergence of the plants.
  • the present invention therefore in particular also relates to a method for the protection of seed and germinating plants, from attack by pests, by treating the seed with one of the compounds of the formula (I).
  • the method according to the invention for protecting seed and germinating plants against attack by pests furthermore comprises a method where the seed is treated simultaneously in one operation or sequentially with a compound of the formula (I) and a mixing component. It also comprises a method where the seed is treated at different times with a compound of the formula (I) and a mixing component.
  • the invention likewise relates to the use of the compounds of the formula (I) for the treatment of seed for protecting the seed and the resulting plant from animal pests.
  • the invention relates to seed which has been treated with a compound of the formula (I) according to the invention so as to afford protection from animal pests.
  • the invention also relates to seed which has been treated simultaneously with a compound of the formula (I) and a mixing component.
  • the invention furthermore relates to seed which has been treated at different times with a compound of the formula (I) and a mixing component.
  • the individual substances may be present on the seed in different layers.
  • the layers comprising a compound of the formula (I) and mixing components may optionally be separated by an intermediate layer.
  • the invention also relates to seed where a compound of the formula (I) and a mixing component have been applied as component of a coating or as a further layer or further layers in addition to a coating.
  • the invention relates to seed which, after the treatment with a compound of the formula (I), is subjected to a film-coating process to prevent dust abrasion on the seed.
  • a systemically acting compound of the formula (I) is the fact that, by treating the seed, not only the seed itself but also the plants resulting therefrom are, after emergence, protected against animal pests. In this manner, the immediate treatment of the crop at the time of sowing or shortly thereafter can be dispensed with. It has to be considered a further advantage that by treatment of the seed with a compound of the formula (I), germination and emergence of the treated seed may be enhanced. It is likewise to be considered advantageous that compounds of the formula (I) can be used in particular also for transgenic seed.
  • compounds of the formula (I) can be employed in combination with compositions or compounds of signalling technology, leading to better colonization by symbionts such as, for example, rhizobia, mycorrhizae and/or endophytic bacteria or fungi, and/or to optimized nitrogen fixation.
  • symbionts such as, for example, rhizobia, mycorrhizae and/or endophytic bacteria or fungi, and/or to optimized nitrogen fixation.
  • the compounds of the formula (I) are suitable for protection of seed of any plant variety which is used in agriculture, in the greenhouse, in forests or in horticulture.
  • this takes the form of seed of cereals (for example wheat, barley, rye, millet and oats), corn, cotton, soya beans, rice, potatoes, sunflowers, coffee, tobacco, canola, oilseed rape, beets (for example sugarbeets and fodder beets), peanuts, vegetables (for example tomatoes, cucumbers, bean, cruciferous vegetables, onions and lettuce), fruit plants, lawns and ornamental plants.
  • cereals for example wheat, barley, rye and oats
  • transgenic seed with a compound of the formula (I) is also of particular importance.
  • the heterologous genes in transgenic seed can originate from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
  • the present invention is particularly suitable for the treatment of transgenic seed which comprises at least one heterologous gene originating from Bacillus sp.
  • the compound of the formula (I) is applied to the seed.
  • the seed is treated in a state in which it is stable enough to avoid damage during treatment.
  • the seed may be treated at any point in time between harvest and sowing.
  • the seed usually used has been separated from the plant and freed from cobs, shells, stalks, coats, hairs or the flesh of the fruits.
  • seed which has been harvested, cleaned and dried down to a moisture content which allows storage.
  • seed which, after drying, has been treated with, for example, water and then dried again, for example priming.
  • the amount of the compound of the formula (I) applied to the seed and/or the amount of further additives is chosen in such a way that the germination of the seed is not adversely affected, or that the resulting plant is not damaged. This must be ensured particularly in the case of active compounds which can exhibit phytotoxic effects at certain application rates.
  • the compounds of the formula (I) are applied to the seed in a suitable formulation. Suitable formulations and processes for seed treatment are known to the person skilled in the art.
  • the compounds of the formula (I) can be converted to the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other coating compositions for seed, and also ULV formulations.
  • These formulations are prepared in a known manner, by mixing the compounds of the formula (I) with customary additives such as, for example, customary extenders and also solvents or diluents, colorants, wetting agents, dispersants, emulsifiers, antifoams, preservatives, secondary thickeners, adhesives, gibberellins and also water.
  • customary additives such as, for example, customary extenders and also solvents or diluents, colorants, wetting agents, dispersants, emulsifiers, antifoams, preservatives, secondary thickeners, adhesives, gibberellins and also water.
  • pigments which are sparingly soluble in water
  • dyes which are soluble in water.
  • examples include the dyes known by the names Rhodamine B, C.I. Pigment Red 112 and C.I. Solvent Red 1.
  • Useful wetting agents which may be present in the seed dressing formulations usable in accordance with the invention are all substances which promote wetting and which are conventionally used for the formulation of agrochemically active compounds. Preference is given to using alkylnaphthalenesulphonates, such as diisopropyl- or diisobutylnaphthalenesulphonates.
  • Useful dispersants and/or emulsifiers which may be present in the seed dressing formulations usable in accordance with the invention are all nonionic, anionic and cationic dispersants conventionally used for the formulation of active agrochemical ingredients. Preference is given to using nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
  • Suitable nonionic dispersants include in particular ethylene oxide/propylene oxide block polymers, alkylphenol polyglycol ethers and tristryrylphenol polyglycol ethers, and the phosphated or sulphated derivatives thereof.
  • Suitable anionic dispersants are in particular lignosulphonates, polyacrylic acid salts and arylsulphonate/formaldehyde condensates.
  • Antifoams which may be present in the seed dressing formulations usable in accordance with the invention are all foam-inhibiting substances conventionally used for the formulation of active agrochemical ingredients. Preference is given to using silicone antifoams and magnesium stearate.
  • Preservatives which may be present in the seed dressing formulations usable in accordance with the invention are all substances usable for such purposes in agrochemical compositions. Examples include dichlorophene and benzyl alcohol hemiformal.
  • the gibberellins are known (cf. R. Wegler "Chemie der convinced für Schweizer- and Schdlingsbehimmpfungsstoff", vol.2, Springer Verlag, 1970, pp.401-412).
  • the seed dressing formulations usable in accordance with the invention can be used to treat a wide variety of different kinds of seed either directly or after prior dilution with water.
  • the concentrates or the preparations obtainable therefrom by dilution with water can be used to dress the seed of cereals, such as wheat, barley, rye, oats, and triticale, and also the seed of maize, rice, oilseed rape, peas, beans, cotton, sunflowers, soya beans and beets, or else a wide variety of different vegetable seed.
  • the seed dressing formulations usable in accordance with the invention, or the dilute use forms thereof can also be used to dress seed of transgenic plants.
  • all mixing units usable customarily for the seed dressing are useful.
  • the procedure in the seed dressing is to place the seed into a mixer, operated batch- wise or continously, to add the particular desired amount of seed dressing formulations, either as such or after prior dilution with water, and to mix everything until the formulation is distributed homogeneously on the seed. If appropriate, this is followed by a drying operation.
  • the application rate of the seed dressing formulations usable in accordance with the invention can be varied within a relatively wide range. It is guided by the particular content of the compounds of the formula (I) in the formulations and by the seed.
  • the application rates of the compound of the formula (I) are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
  • Animal health In the animal health field, i.e.
  • the compounds of the formula (I) are active against animal parasites, in particular ectoparasites or endoparasites.
  • Ectoparasites are typically and preferably arthropods, in particular insects or acarids.
  • the compounds of the formula (I) are suitable, with favourable toxicity in warm blooded animals, for controlling parasites which occur in animal breeding and animal husbandry in livestock, breeding, zoo, laboratory, experimental and domestic animals (companion animals). They are active against all or specific stages of development of the parasites.
  • Agricultural livestock include, for example, mammals, such as, sheep, goats, horses, donkeys, camels, buffaloes, rabbits, reindeers, fallow deers, and in particular cattle and pigs; or poultry, such as turkeys, ducks, geese, and in particular chickens; or fish or crustaceans, e.g. in aquaculture; or, as the case may be, insects such as bees.
  • Domestic animals or companion animals include, for example, mammals, such as hamsters, guinea pigs, rats, mice, chinchillas, ferrets or in particular dogs, cats; cage birds; reptiles; amphibians or aquarium fish.
  • the compounds of the formula (I) are administered to mammals.
  • the compounds of the formula (I) are administered to birds, namely cage birds or in particular poultry.
  • the compounds of the formula (I) are administered to farm animals or companion animals, in particular to companion animals such as cats and dogs.
  • control means that the compounds of the formula (I) are effective in reducing the incidence of the respective parasite in an animal infected with such parasites to innocuous levels. More specifically, “controlling”, as used herein, means that the compounds of the formula (I) are effective in killing the respective parasite, inhibiting its growth, or inhibiting its proliferation.
  • Exemplary arthropods include, without any limitation from the order of the Anoplurida, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.; from the order of the Mallophagida and the suborders Amblycerina and Ischnocerina, for example Bovicola spp., Damalina spp., Felicola spp., Lepikentron spp., Menopon spp., Trichodectes spp., Trimenopon spp., Trinoton spp., Werneckiella spp.; from the order of the Diptera and the suborders Nematocerina and Brachycerina, for example Aedes spp., Anopheles spp., Atylotus spp., Braula spp., Calliphora spp., Chr
  • Siphonapta for example Ceratophyllus spp.; Ctenocephalides spp., Pulex spp., Tunga spp., Xenopsylla spp.; from the order of the Heteropterida, for example Cimex spp., Panstrongylus spp., Rhodnius spp., Triatoma spp.; as well as nuisance and hygiene pests from the order of the Blattarida.
  • acari may be mentioned by way of example, without any limitation: from the subclass of the Acari (Acarina) and the order of the Metastigmata, for example, from the family of argasidae like Argas spp., Ornithodorus spp., Otobius spp., from the family of Ixodidae like Amblyomma spp., Dermacentor spp., Haemaphysalis spp., Hyalomma spp., Ixodes spp., Rhipicephalus (Boophilus) spp , Rhipicephalus spp.
  • the compounds of the formula (I) are effective in reducing the incidence of parasites selected from arthropods, more particularly from the subclass of the Acari and insects, in an animal infected with such parasites to innocuous levels.
  • the administration of the compounds of the formula (I) is carried out by methods generally known in the art, such as enterally, parenterally, dermally or nasally, in the form of suitable preparations. Administration can be carried out prophylactically, methaphylactically or therapeutically.
  • one embodiment of the present invention refers to the compounds of the formula (I) for use as a medicament.
  • Another aspect refers to the compounds of the formula (I) for use as an antiendoparasitical agent.
  • Another aspect refers to the compounds of the formula (I) for use as an antiectoparasitical agent, in particular an arthropodicidal agent, more particular an insecticidal agent or acaricidal agent.
  • veterinary formulations comprising an effective amount of at least one compound of the formula (I) and at least one of the following: pharmaceutically acceptable excipient (e.g. solid or liquid diluents), pharmaceutically acceptable auxiliary (e.g. surfactants), in particular a pharmaceutically acceptable excipient and/or pharmaceutically acceptable auxiliary which is normally used in veterinary formulations.
  • a related aspect of the invention is a method for preparing a veterinary formulation as described herein, comprising the step of mixing at least one compound of the formula (I) with pharmaceutically acceptable excipients and/or auxiliaries , in particular with pharmaceutically acceptable excipients and/or auxiliaries which are normally used in veterinary formulations.
  • veterinary formulations selected from the group of ectoparasiticidal and endoparasiticidal formulations, more particular an arthropodicidal formulations, even more particular selected from the group of nematicidal, platyhelminthicidal, acanthocephalicidal, pentastomicidal, insecticidal, and acaricidal formulations, in accordance with the mentioned aspects, as well as their methods for preparation.
  • Another aspect refers to a method for treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, by applying an effective amount of a compound of the formula (I) to an animal, in particular a non-human animal, in need thereof.
  • Another aspect refers to a method for treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, by applying a veterinary formulation as defined herein to an animal, in particular a non-human animal, in need thereof.
  • Another aspect refers to the use of the compounds of the formula (I) in the treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, in an animal, in particular a non-human animal.
  • treatment includes prophylactic, metaphylactic or therapeutical treatment.
  • mixtures of at least one compound of the formula (I) with other active ingredients, particularly with endo- and ectoparasiticides, for the veterinary field are provided herewith.
  • mixture not only means that two (or more) different active ingredients are formulated in a joint formulation and are accordingly applied together but also refers to products which comprise separate formulations for each active compound. Accordingly, if more than two active compounds are to be applied, all active compounds may be formulated in a joint formulation or all active compounds may be formulated in separate formulations; also feasible are mixed forms where some of the active compounds are formulated jointly and some of the active compounds are formulated separately. Separate formulations allow the separate or successive application of the active compounds in question.
  • the active compounds specified herein by their common names are known and described, for example, in the Pesticide Manual (see above) or can be searched in the internet (e.g. http://www.alanwood.net/pesticides).
  • Exemplary active ingredients from the group of ectoparasiticides, as mixing partners, include, without limitation insecticides and acaricides listed in detail above. Further active ingredients which may be used are listed below following the aforementioned classification which is based on the current IRAC Mode of Action Classification Scheme: (1) Acetylcholinesterase (AChE) inhibitors; (2) GABA-gated chloride channel blockers; (3) Sodium channel modulators; (4) Nicotinic acetylcholine receptor (nAChR) competitive modulators; (5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators; (6) Glutamate-gated chloride channel (GluCl) allosteric modulators; (7) Juvenile hormone mimics; (8) Miscellaneous non-specific (multi-site) inhibitors; (9) Modulators of Chordotonal Organs; (10) Mite growth inhibitors; (12) Inhibitors of mitochondrial ATP synthase, such as, ATP disruptors;
  • camphechlor lindane, heptachlor; or phenylpyrazoles, e.g. acetoprole, pyrafluprole, pyriprole, vaniliprole, sisapronil; or isoxazolines, e.g. sarolaner, afoxolaner, lotilaner, fluralaner; pyrethroids, e.g.
  • nithiazine dicloromezotiaz triflumezopyrim macrocyclic lactones, e.g. nemadectin, ivermectin, latidectin, moxidectin, selamectin, eprinomectin, doramectin, emamectin benzoate; milbemycin oxime triprene, epofenonane, diofenolan; Biologicals, hormones or pheromones, for example natural products, e.g. thuringiensin, codlemone or neem components dinitrophenols, e.g.
  • dinocap, dinobuton, binapacryl e.g. benzoylureas, e.g. fluazuron, penfluron, amidine derivatives, e.g. chlormebuform, cymiazole, demiditraz Bee hive varroa acaricides, for example organic acids, e.g. formic acid, oxalic acid.
  • active ingredients from the group of endoparasiticides, as mixing partners include, without limitation, anthelmintically active compounds and antiprotozoal active compounds.
  • Anthelmintically active compounds including, without limitation, the following nematicidally, trematicidally and/or cestocidally active compounds: from the class of macrocyclic lactones, for example: eprinomectin, abamectin, nemadectin, moxidectin, doramectin, selamectin, lepimectin, latidectin, milbemectin, ivermectin, emamectin, milbemycin; from the class of benzimidazoles and probenzimidazoles, for example: oxibendazole, mebendazole, triclabendazole, thiophanate, parbendazole, oxfendazole, netobimin, fenbendazole, febantel, thiabendazole, cyclobendazole, cambendazole, albendazole-sulphoxide, albendazole, flu
  • Antiprotozoal active compounds including, without limitation, the following active compounds: from the class of triazines, for example: diclazuril, ponazuril, letrazuril, toltrazuril; from the class of polylether ionophore, for example: monensin, salinomycin, maduramicin, narasin; from the class of macrocyclic lactones, for example: milbemycin, erythromycin; from the class of quinolones, for example: enrofloxacin, pradofloxacin; from the class of quinines, for example: chloroquine; from the class of pyrimidines, for example: pyrimethamine; from the class of sulfonamides, for example: sulfaquinoxaline, trimethoprim, sulfaclozin; from the class of thiamines, for example: amprolium; from the class of lincosamides, for example: clindamycin
  • a vector is an arthropod, in particular an insect or arachnid, capable of transmitting pathogens such as, for example, viruses, worms, single-cell organisms and bacteria from a reservoir (plant, animal, human, etc.) to a host.
  • pathogens can be transmitted either mechanically (for example trachoma by non-stinging flies) to a host, or by injection (for example malaria parasites by mosquitoes) into a host.
  • vectors and the diseases or pathogens they transmit are: 1) Mosquitoes - Anopheles: malaria, filariasis; - Culex: Japanese encephalitis, other viral diseases, filariasis, transmission of other worms; - Aedes: yellow fever, dengue fever, other viral diseases, filariasis; - Simuliidae: transmission of worms, in particular Onchocerca volvulus; - Psychodidae: transmission of leishmaniasis 2) Lice: skin infections, epidemic typhus; 3) Fleas: plague, endemic typhus, cestodes; 4) Flies: sleeping sickness (trypanosomiasis); cholera, other bacterial diseases; 5) Mites: acariosis, epidemic typhus, rickettsialpox, tularaemia, Saint Louis encephalitis, tick-borne encephalitis (TBE), Crimean–Congo haemorrhagic fever, borreliosis;
  • vectors in the sense of the present invention are insects, for example aphids, flies, leafhoppers or thrips, which are capable of transmitting plant viruses to plants.
  • Other vectors capable of transmitting plant viruses are spider mites, lice, beetles and nematodes.
  • Further examples of vectors in the sense of the present invention are insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, for example A. gambiae, A. arabiensis, A. funestus, A.
  • a further aspect of the present invention is the use of compounds of the formula (I) for vector control, for example in agriculture, in horticulture, in gardens and in leisure facilities, and also in the protection of materials and stored products.
  • the compounds of the formula (I) are suitable for protecting industrial materials against attack or destruction by insects, for example from the orders Coleoptera, Hymenoptera, Isoptera, Lepidoptera, Psocoptera and Zygentoma.
  • Industrial materials in the present context are understood to mean inanimate materials, such as preferably plastics, adhesives, sizes, papers and cards, leather, wood, processed wood products and coating compositions. The use of the invention for protecting wood is particularly preferred.
  • the compounds of the formula (I) are used together with at least one further insecticide and/or at least one fungicide.
  • the compounds of the formula (I) are present as a ready-to-use pesticide, i.e.
  • the compounds of the formula (I) can be employed for protecting objects which come into contact with saltwater or brackish water, in particular hulls, screens, nets, buildings, moorings and signalling systems, against fouling.
  • the compounds of the formula (I) alone or in combinations with other active compounds, can be used as antifouling agents. Control of animal pests in the hygiene sector
  • the compounds of the formula (I) are suitable for controlling animal pests in the hygiene sector.
  • the invention can be applied in the domestic sector, in the hygiene sector and in the protection of stored products, especially for controlling insects, arachnids, ticks and mites encountered in enclosed spaces such as dwellings, factory halls, offices, vehicle cabins, animal husbandries.
  • the compounds of the formula (I) are used alone or in combination with other active compounds and/or auxiliaries. They are preferably used in domestic insecticide products.
  • the compounds of the formula (I) are effective against sensitive and resistant species, and against all developmental stages.
  • pests from the class Arachnida from the orders Scorpiones, Araneae and Opiliones, from the classes Chilopoda and Diplopoda, from the class Insecta the order Blattodea, from the orders Coleoptera, Dermaptera, Diptera, Heteroptera, Hymenoptera, Isoptera, Lepidoptera, Phthiraptera, Psocoptera, Saltatoria or Orthoptera, Siphonaptera and Zygentoma and from the class Malacostraca the order Isopoda.
  • Scheme 1 The synthesis starts with a pyrazine of formula (II) which carries residues R 5 and R 6 , as well as one group X 1 which can be chlorine, bromine or iodine. These compounds are commercially available or can be made according to methods described in the art.
  • the hydrogen atom next to X 1 is abstracted and replaced by a metal fragment consisting of a main group metal such as Li, Mg, Zn and appropriate ligands L.
  • a metal fragment consisting of a main group metal such as Li, Mg, Zn and appropriate ligands L.
  • An example for such a transformation is given by F. Buron, N. Pié, A. Turck, G, Quéguigner, J. Org.
  • Metalation and reaction with the aldehyde are typically carried out in one pot in a polar, nonprotic solvent such as THF, diethyl ether, dioxane.
  • a polar, nonprotic solvent such as THF, diethyl ether, dioxane.
  • the temperature in the metalation step is typically below 0 °C, preferably at -78 °C in a dry ice bath. After the addition of the aldehyde, the temperature may be raised to 0 °C or even room temperature.
  • the organometal intermediate may also be prepared in advance and then be added to a solution of the aldehyde in a suitable nonprotic solvent such as, for instance, THF, ether or toluene.
  • the subsequent step consists in the replacement of the hydroxy group from intermediate (V) by a fully protected nitrogen resulting in intermediates of formula (VII).
  • PG 1 and PG 2 may be either two independent protecting groups or may be joined to form one cyclic protecting group. Depending on the respective reaction and the protecting group used the other of PG 1 and PG 2 may also represent hydrogen. Examples for protecting groups suitable for the protection of amino functionalities can be found in T.W. Greene, P.G.M. Wuts “Protective Groups in Organic Chemistry” 3 rd edition, Wiley Interscience, New York 1999, e.g. the Boc-group. Preferentially, the phthalimide protecting group is used.
  • the replacement of the hydroxy group may be carried out either by converting the alcohol into a halogenide by a method known in the art, e.g. Appel reaction, treatment with sulfuryl chloride etc and subsequent nucleophilic substitution by phthalimide, or, preferably, by direct conversion of intermediate (V) with phthalimide in a Mitsunobu reaction with DIAD and triphenylphosphine a in a suitable solvent such as THF at temperature ranging from -40 °C to 100 °C, preferentially from 0 °C to room temperature.
  • Introduction of R 4 occurs in the next step using a cross coupling reaction with reagent (VIII) which carries the leaving group X 2 .
  • X 2 may be a trialkyl stannyl residue, a boronic acid, a boronic ester or a metal fragment M(Ln) with a metal such as Ni, Zn, Mg and appropriate ligands L.
  • the cross coupling reaction is typically catalyzed by a transition metal catalyst such as a palladium or copper catalyst with appropriate ligands.
  • a transition metal catalyst such as a palladium or copper catalyst with appropriate ligands.
  • a variation of the cross coupling reaction could be to replace the moiety X 1 from intermediate (VII) by a trialkyl trialkyl stannyl residue, a boronic acid, a boronic ester or a metal fragment M(L n ) with a metal such as Ni, Zn, Mg and appropriate ligands L.
  • intermediate (VIII) would have to carry a group X 2 chosen from, for instance, Cl, Br, I, triflate or similar.
  • Ligands can be chosen from phosphine ligands or N-heterocyclic carbene ligands, an overview of some ligands is given in R. Martin, S.L. Buchwald, Acc. Chem. Res.2008, 61, 1461-1473.
  • the product (IX) of the cross coupling reaction has to be deprotected in the next step.
  • a phthalimide protecting group is used, this can be achieved by reacting (IX) with hydrazine hydrate in an appropriate solvent such as ethanol at room temperature or above room temperature.
  • Compounds of formula (I) can be obtained by reacting intermediates (X) with carboxylic acid derivatives (XI) wherein X 3 is Cl, O-acyl or OH.
  • X is Cl or O-acyl
  • (X) and (XI) are directly reacted in the presence of a base such as, for instance, DIPEA, triethylamine or N-methylmorpholine in a solvent such as DMF, THF or similar.
  • the acid (XI) needs to be activated using a coupling agent such as HATU, TBTU, TCTU, PyBOP etc or, alternatively, converting it into the corresponding acid chloride or an anhydride prior to react it with (X) as described above.
  • the resulting products (Ia) are compounds of the invention where R 1 is H.
  • an alkylation reaction with alkylating agent (XII) may be used. Examples of leaving groups LG are Cl, Br, I, tosylate, mesylate or triflate groups.
  • the reaction may be carried out by mixing the reagents (Ia) and (XII) together with a base, such as K2CO3 or DIPEA in a suitable solvent, such as acetonitrile or DMF and letting them react at a temperature in the range 20 to 100 °C.
  • a base such as K2CO3 or DIPEA
  • a suitable solvent such as acetonitrile or DMF
  • Compounds of formula (Ib) may then be isolated and, if necessary and desired, purified using techniques well known in the art, such as chromatography. If in the compounds (I) R 4 is a pyridine-group, then it is preferred that in the Scheme 1 supra X 1 is Cl, X 2 is Zn-Cl, the Pd-catalyst is a Pd2(dba)3 catalyst and the ligand L is X-Phos.
  • the general strategy for these molecules may follow the order of steps displayed in either Scheme 1 or Scheme 2.
  • the introduction of a pyrazole or imidazole is carried out prior to the introduction of the amine as shown in Scheme 2.
  • the actual cross coupling step is carried out using a metal catalyst, optionally ligands, a base and a solvent.
  • Metal catalysts useful in this step comprise copper(I) and copper(II) salts, preferentially copper(I) halides such as, for instance, copper(I) iodide.
  • the use of a ligand may be beneficial, the choice of a suitable ligand depends on the metal catalyst.
  • 1,2- diamines such as TMEDA or trans-N,N,N',N'-tetramethylcyclohexane-1,2-diamine are used.
  • a catalytic amount of the metal catalyst and the ligand is used, typically in the range of 0.01-0.5 molar equivalents of each of them.
  • alkali or earth alkali carbonates may be used such as, for instance, calcium carbonate, sodium carbonate, potassium carbonate or cesium carbonate.
  • Solvents include DMF, THF, 1,4- dioxane toluene, chlorobenzene or other organic solvents usually employed for cross coupling reactions.
  • the reaction is performed at room temperature or above, preferrably at 100-120 °C.
  • the preferred conditions for cross coupling comprise using 0.3 equiovalents of copper(I) iodide, 0.3 eqivalents of trans-N,N,N',N'-tetramethylcyclohexane-1,2-diamine, an excess of potassium carbonate in toluene under reflux.
  • compounds of the invention are accessible via modifications of the substituents in the aftermath of the introduction of R 4 . These operations can be carried out either in the presence of the R 2 moiety or, as an alternative, prior to the introduction of R 2 using a suitably protected intermediate according to formula IX (see Scheme I).
  • an ester group placed on R 4 may be saponified by standard methodology.
  • Preferred methods for the saponification of esters comprise lithium hydroxide or sodium hydroxide in a mixture of solvents such as methanol and THF with water at a temperature ranging from room temperature to reflux, or lithium iodide in pyridine at a temperature above 100 °C.
  • the resulting carboxylic acid can be converted into carboxamides by the use of coupling agents such as TBTU, HATU, EDCI or other reagents known in the art.
  • Carboxylic esters can also be converted into cyanides using Burgess reagent.
  • carboxylic acids can be converted into amines using a Curtius rearrangement, and the resulting amino group can then be acylated to give a carboxamide linked to R 4 via a nitrogen atom by the use of coupling agents such as TBTU, HATU, EDCI or other reagents known in the art.
  • the processes according to the invention for the preparation of compounds of the formula (I) are preferably performed using a diluent.
  • Useful diluents for performance of the processes according to the invention are, as well as water, all inert solvents.
  • halohydrocarbons for example chlorohydrocarbons such as tetrachloroethylene, tetrachloroethane, dichloropropane, methylene chloride, dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichloroethylene, pentachloroethane, difluorobenzene, 1,2-dichloroethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene), alcohols (for example methanol, ethanol, isopropanol, butanol), ethers (for example ethyl propyl ether, methyl tert-butyl ether, anisole, phenetole, cyclohexyl methyl ether, dimethyl ether, diethyl ether, dipropyl ether, diisopropyl ether
  • the reaction temperatures can be varied within a relatively wide range. In general, the temperatures employed are between -30 °C and +150 °C, preferably between -10 °C and +100 °C.
  • the process according to the invention is generally performed under atmospheric pressure. However, it is also possible to perform the process according to the invention under elevated or reduced pressure – generally at absolute pressures between 0.1 bar and 15 bar.
  • the starting materials are generally used in approximately equimolar amounts. However, it is also possible to use one of the components in a relatively large excess.
  • the reaction is generally carried out in a suitable diluent in the presence of a reaction auxiliary, optionally also under a protective gas atmosphere (for example under nitrogen, argon or helium) and the reaction mixture is generally stirred at the temperature required for several hours.
  • a reaction auxiliary optionally also under a protective gas atmosphere (for example under nitrogen, argon or helium) and the reaction mixture is generally stirred at the temperature required for several hours.
  • the workup is performed by customary methods (cf. the preparation examples).
  • the basic reaction auxiliaries used to perform the process according to the invention may be all suitable acid binders. Examples include: alkaline earth metal or alkali metal compounds (e.g. hydroxides, hydrides, oxides and carbonates of lithium, sodium, potassium, magnesium, calcium and barium), amidine bases or guanidine bases (e.g.
  • the acidic reaction auxiliaries used to perform the process according to the invention include all mineral acids (e.g. hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid or hydriodic acid, and also sulphuric acid, phosphoric acid, phosphorous acid, nitric acid), Lewis acids (e.g. aluminium(III) chloride, boron trifluoride or its etherate, titanium(IV) chloride, tin(IV) chloride) and organic acids (e.g.
  • mineral acids e.g. hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid or hydriodic acid, and also sulphuric acid, phosphoric acid, phosphorous acid, nitric acid
  • Lewis acids e.g. aluminium(III) chloride, boron trifluoride or its etherate, titanium(IV) chloride, tin(IV) chloride
  • organic acids e.g.
  • Method 8 (optical rotation) Device: Anton Paar Polarimeter MCP200 Specific rotation [ ⁇ ] (depending wavelength, temperature, optical pathway, solvent and concentration).
  • n- Butyllithium (2.5 M in hexanes, 1.2 equivalents) was slowly added over 90 min. Stirring at -78 °C was maintained for another 60 min, then the cooling bath was removed and the mixture was left to warm to ambient temperature.
  • a solution of 2,2'-(methylimino)diacetic acid (1.6 equivalents) in DMSO (dried over 3 ⁇ molecular sieves, 150 mL) was heated to 125-130 °C. The suspension of the boronate in THF was slowly added over approximately 2 h distilling off the THF and keeping the temperature in a range between 115-125 °C.
  • the reaction was allowed to warm to ambient temperature and was stirred for 2 h.
  • the solvent was distilled and the residue was directly charged onto a silica gel column (100 g of silica gel) and chromatographed using a gradient of cyclohexane and 0-35% ethyl acetate.5.37 g (98 % purity, 63 % yield) of the title compound were obtained.
  • Solution B Pd 2 (dba) 3 (18.3 mg, 20.0 ⁇ mol) and dicyclohexyl[2',4',6'-tri(propan-2-yl)biphenyl-2- yl]phosphane (XPhos, 38.1 mg, 80.0 ⁇ mol) were dissolved in THF (2.0 mL). This mixture was heated to 65 °C for 10 min, then (rac)-2-[1-(3-chloropyrazin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (intermediate 2A, 288 mg, 1.00 mmol) was added and stirring at 65 °C was continued for another 15 min.
  • (+)-2-(3- ⁇ (1S)-1-[(tert-Butoxycarbonyl)amino]ethyl ⁇ pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid (intermediate 43A, 825 mg, 2.35 mmol) was dissolved in DMF (19.0 mL) and the solution was cooled to 0 °C.
  • N-Methylethanamine 300 ⁇ l, 3.5 mmol
  • DIPEA 1.6 ml, 9.4 mmol
  • Example I-1 (rac)-3-Chloro-N- ⁇ 1-[3-(pyridin-2-yl)pyrazin-2-yl]ethyl ⁇ -5-(trifluoromethyl)benzamide
  • (rac)-1-[3-(Pyridin-2-yl)pyrazin-2-yl]ethan-1-amine (intermediate 4A, 66.1 mg, 330 ⁇ mol) was dissolved in DMF (3.5 mL), HATU (188 mg, 495 ⁇ mol), 3-chloro-5-(trifluoromethyl)benzoic acid (81.5 mg, 363 ⁇ mol) and DIPEA (170 ⁇ l, 990 ⁇ mol) were added and the mixture was stirred at room temperature for 45 min.
  • reaction mixture was directly charged onto a preparative HPLC and purified using RP C-1810 ⁇ m material and a gradient water (+0.1% TFA) – acetonitrile (+0.1% TFA) 90:10->5:95). 67.0 mg (94 % purity, 47 % yield) of the title compound were obtained.
  • Example I-3 (rac)-3-Chloro-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
  • Example I-4 (rac)-3-Fluoro-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
  • Example I-5 (rac)-N-(1-(3-(Thiazol-2-yl)pyrazin-2-yl)ethyl)-3,5-bis(trifluoromethyl)benzamide
  • Example I-6 (rac)-5-(tert-Butyl)-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)nicotinamide
  • 5-tert-butylnicotinic acid (intermediate 7A, 40 mg, 0.22 mmol) in N,N- dimethylformamide (5 mL) was added (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A, 46 mg, 0.22 mmol), HATU (127 mg, 0.34 mmol), and N,N-diisopropylethylamine (87 mg, 0.67 mmol).
  • Example I-7 (rac)-3-Fluoro-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
  • Example I-8 (rac)-N-(1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethyl)-3,5-bis(trifluoromethyl)benzamide
  • the resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with dichloromethane.
  • Example I-9 (rac)-N-(1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)nicotinamide
  • Example I-10 (rac)-3-Chloro-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
  • Example I-11 (rac)-5-(tert-Butyl)-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)nicotinamide
  • 5-tert-butylnicotinic acid 40 mg, 0.22 mmol
  • N,N-dimethylformamide 5 mL
  • was added (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 45 mg, 0.22 mmol), HATU (127 mg, 0.34 mmol), and N,N-diisopropylethylamine (87 mg, 0.67 mmol).
  • Example I-30 (rac)-Methyl 6-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3- carboxylate (rac) 6- ⁇ 3-[1-aminoethyl]pyrazin-2-yl ⁇ pyridine-3-carboxylate (intermediate 25A, 130 mg, 503 ⁇ mol), 3,5-bis(trifluoromethyl)benzoic acid (169 mg, 654 ⁇ mol) and DIPEA (260 ⁇ l, 1.5 mmol) were dissolved in DMF (3.0 mL).
  • Example I-31 (rac)-6-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3-carboxylic acid (rac)-Methyl 6-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3-carboxylate (example I-30, 185 mg, 371 ⁇ mol) was suspended in methanol (3.0 mL) and a previously prepared solution of sodium hydroxide (104 mg, 2.61 mmol) in water (1.0 mL) was added at ambient temperature. The mixture was stirred for 30 min.
  • reaction mixture was then diluted with water, acidified with 1 M hydrochloric acid and extracted with three portions of ethyl acetate.
  • the combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, evaporated and eventually purified by preparative HPLC (RP-C18, water-acetonitril gradient with 0.1% TFA).
  • a yield of 153 mg (100 % purity, 85 % of theory) of the title compound was isolated.
  • Example I-32 (rac)-6-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methylpyridine-3-carboxamide (rac)-6-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3-carboxylic acid (70.0 mg, 145 ⁇ mol) was dissolved in DMF (2.0 mL). 1-cyclopropyl-N-methylmethanamine hydrogen chloride (26.4 mg, 217 ⁇ mol) and DIPEA (130 ⁇ l, 720 ⁇ mol) were added.
  • Example I-49 (rac)-Methyl 2-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1,3-thiazole-5- carboxylate
  • (rac)-Methyl 2- ⁇ 3-[1-aminoethyl]pyrazin-2-yl ⁇ -1,3-thiazole-5-carboxylate (intermediate 28A, 300 mg, 1.14 mmol) and DIPEA (400 ⁇ L, 2.3 mmol) were dissolved in THF (15.0 mL) and cooled to 0 °C.
  • Example I-50 (rac)-2-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid (rac)-Methyl 2-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1,3-thiazole-5- carboxylate (example I-49, 570 mg, 1.13 mmol) was suspended in a mixture of methanol (15.0 mL), THF (5.0 mL) and water (5.0 mL).
  • Example I-51 (rac)-2-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methyl-1,3-thiazole-5-carboxamide (rac)-2-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid (example I-50, 100 mg, 204 ⁇ mol) was dissolved in DMF (3.6 mL).
  • Example I-83 (rac)-2- ⁇ 3-[1- ⁇ [3,5-Bis(trifluoromethyl)benzoyl](cyclopropylmethyl)amino ⁇ ethyl]pyrazin-2-yl ⁇ -N- ethyl-N-methyl-1,3-thiazole-5-carboxamide (rac)-2-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N-ethyl-N-methyl-1,3-thiazole-5- carboxamide (example 72, 196 mg, 369 ⁇ mol) was dissolved in DMF (4.0 mL) and sodium hydride (22.1 mg, 60 % in paraffin, 553 ⁇ mol) was added.
  • Example I-84 Yield: 121 mg (30%) eluting at 5.16 min in the preparative HPLC.
  • Example I-86 (rac)-Ethyl 1-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1H-pyrazole-4- carboxylate
  • (rac)-Ethyl 1- ⁇ 3-[1-aminoethyl]pyrazin-2-yl ⁇ -1H-pyrazole-4-carboxylate (intermediate 37A, 330 mg, 1.26 mmol), 3,5-bis(trifluoromethyl)benzoic acid (424 mg, 1.64 mmol) and DIPEA (660 ⁇ l, 3.8 mmol) were dissolved in DMF (5.0 mL).
  • Example I-87 (rac)-1-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1H-pyrazole-4-carboxylic acid (rac)-Ethyl 1-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1H-pyrazole-4-carboxylate (example I-86, 555 mg, 1.11 mmol) was suspended in a mixture of THF (4.0 mL), ethanol (4.0 mL) and water (1.0 mL).
  • Example I-88 (rac)-1-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N,N-dimethyl-1H-pyrazole- 4-carboxamide (rac)-1-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-1H-pyrazole-4-carboxylic acid (example I-87,105 mg, 222 ⁇ mol), N-methylmethanamine hydrogen chloride (27.1 mg, 333 ⁇ mol) and DIPEA (190 ⁇ l, 1.1 mmol) were dissolved in DMF (2.0 mL).
  • reaction mixture was purified via prep-HPLC [RP-C18, mobile Phase A: water(0.1% TFA), mobile Phase B: acetonitrile; gradient: 65% B to 75% B in 10 min] to give 70 mg of the mixture of enantiomers as a white solid.
  • Example I-162 6-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N-(cyanomethyl)-N- methylpyridine-3-carboxamide (Enantiomer 1) To a solution of (rac)-6-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3- carboxylic acid (example I-31, 80 mg, 0.17 mmol), 2-(methylamino)acetonitrile(18 mg, 0.25 mmol) in N,N-dimethylformamide (6 ml) was added N,N-diisopropylethylamine (107 mg, 0.83 mmol) and HATU (94 mg,0.25 mmol) respectively.
  • reaction mixture was purified via prep-HPLC [mobile phase A: water(0.1% TFA), mobile phase B: acetonitrile; gradient: 65% B to 75% B in 10 min] to give 40 mg of the mixture of enantiomers as a white solid.
  • Example I-163 6-(3- ⁇ 1-[3,5-bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)-N-(cyanomethyl)-N- methylpyridine-3-carboxamide (Enantiomer 2)
  • the title compound was obtained as the second isomer from the chiral chromatography described under example I-162 (16.9 mg, 19% yield) as a pink solid (eluting at 6.687 min in chiral prep HPLC).
  • Example I-166 N-[1-(3- ⁇ 5-[(cis)-2,6-Dimethylmorpholine-4-carbonyl]pyridin-2-yl ⁇ pyrazin-2-yl)ethyl]-3,5- bis(trifluoromethyl)benzamide (Enantiomer 1) enantiomer
  • (rac)-6-(3- ⁇ 1-[3,5-Bis(trifluoromethyl)benzamido]ethyl ⁇ pyrazin-2-yl)pyridine-3- carboxylic acid (example I-31, 80 mg,0.17 mmol)
  • (cis)-2,6-dimethylmorpholine (28 mg, 0.25 mmol) in N,N-dimethylformamide (6 ml) was added N,N-diisopropylethylamine (107 mg, 0.83 mmol) and HATU (94 mg,0.25 mmol) respectively.
  • reaction mixture was purified via prep-HPLC [Mobile Phase A: Water(0.1%FA), Mobile Phase B: ACN; Gradient: 65% B to 75% B in 10 min] to give 67 mg of the mixture of enantiomers as an off-white solid.
  • Example I-167 N-[1-(3- ⁇ 5-[(cis)-2,6-Dimethylmorpholine-4-carbonyl]pyridin-2-yl ⁇ pyrazin-2-yl)ethyl]-3,5- bis(trifluoromethyl)benzamide (Enantiomer 2) enantiomer
  • the title compound was obtained as the second isomer from the chiral chromatography described under example I-166 (19.5 mg 20% yield) as an off-white solid (eluting at 7.081 min in chiral Prep HPLC).
  • each test tube is filled with 20-50 cattle tick larvae (Rhipicephalus microplus), closed with a perforated lid and incubated in a horizontal position at 85 % relative humidity and 27 °C in an incubator. After 48 hours efficacy is determined. The larvae are patted on the ground of the tubes and negative geotactic behaviour is recorded. Larvae that climb back to the top of the vial in a manner comparable to untreated control larvae are marked as alive, larvae not climbing back up comparable to untreated control larvae but are moving uncoordinatedly or only twitching their legs are marked as moribund, tick larvae remaining on the bottom and not moving at all are counted as dead.
  • a compound shows a good efficacy against Rhipicephalus microplus, if at a compound concentration of 5 ⁇ g/cm2 an efficacy of at least 80 % is monitored.
  • An efficacy of 100 % means all larvae are dead or moribund; 0 % means no larvae are dead or moribund.
  • Rhipicephalus (Boophilus) microplus – injection test Solvent dimethyl sulfoxide
  • solvent dimethyl sulfoxide
  • To produce a suitable preparation of active compound 10 mg of active compound are dissolved in 0.5 mL solvent, and the concentrate is diluted with solvent to the desired concentration.
  • Five adult engorged female ticks (Rhipicephalus microplus) are injected with 1 ⁇ L compound solution into the abdomen. The ticks are transferred into replica plates and incubated in a climate chamber. After 7 days egg deposition of fertile eggs is monitored. Eggs where fertility is not visible are stored in a climate chamber till hatching after about 42 days.
  • An efficacy of 100 % means all eggs are infertile; 0 % means all eggs are fertile.
  • the following compounds from the preparation examples showed good activity of 100 % at an application rate of 4 ⁇ g/animal: I-2, I-3, I-7, I-8, I-9, I-10, I-17, I-23, I-24, I-56, I-63, I- 64.
  • the following compounds from the preparation examples showed good activity of 80 % at an application rate of 4 ⁇ g/animal: I-5, I-13, I-14, I-15, I-20, I-21, I-25, I-53, I-65, I-66.
  • Ctenocephalides felis – in-vitro contact tests adult cat flea 9 mg compound is solved in 1 ml acetone and diluted with acetone to the desired concentration.250 ⁇ L of the test solution is filled in 25 mL glass test tubes and homogeneously distributed on the inner walls by rotation and tilting on a shaking device (2 h at 30 rpm). With a compound concentration of 900 ppm, an inner surface of 44.7 cm 2 and a homogeneous distribution, a dose of 5 ⁇ g/cm2 is achieved. After the solvent has evaporated, each test tube is filled with 5-10 adult cat fleas (Ctenocephalides felis), closed with a perforated lid and incubated in a lying position at room temperature and relative humidity.
  • the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 ppm: I-7, I-8, I-10, I-12, I-14, I-15, I-16, I-17, I-23, I-24, I-55.
  • the following compounds from the preparation examples showed good activity of 90 % at an application rate of 100 ppm: I-1, I-2, I-3, I-5, I-11, I-13, I-25.
  • the following compounds from the preparation examples showed good activity of 80 % at an application rate of 100 ppm: I-9, I-65.
  • Rhipicephalus sanguineus - in-vitro contact tests with adult brown dog ticks 9 mg compound is solved in 1 mL acetone and diluted with acetone to the desired concentration.250 ⁇ L of the test solution is filled in 25 mL glass test tubes and homogeneously distributed on the inner walls by rotation and tilting on a shaking device (2 h at 30 rpm). With a compound concentration of 900 ppm, an inner surface of 44.7 cm 2 and a homogeneous distribution, a dose of 5 ⁇ g/cm2 is achieved.
  • each test tube is filled with 5-10 adult brown dog ticks (Rhipicephalus sanguineus), closed with a perforated lid and incubated in a lying position at room temperature and relative humidity. After 48 hours efficacy is determined. The ticks are patted on the ground of the tubes and are incubated on a heating plate at 45-50 °C for at most 5 minutes. Immotile or uncoordinated moving ticks, which are not able to escape the heat by climbing upwards, are marked as dead or moribund. A compound shows a good efficacy against Rhipicephalus sanguineus, if at a compound concentration of 5 ⁇ g/cm2 an efficacy of at least 80 % is monitored.
  • an efficacy of 100 % means all ticks are dead or moribund; 0 % means no ticks are dead or moribund.
  • Diabrotica balteata – spray test Solvent: 78.0 parts by weight of acetone 1.5 parts by weight of dimethylformamide
  • Emulsifier alkylarylpolyglycol ether
  • To produce a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Soaked wheat seeds (Triticum aestivum) are placed in a multiple well plate filled with agar and some water and are incubated for 1 day to germinate (5 seeds per well).
  • the germinated wheat seeds are sprayed with a test solution containing the desired concentration of the active ingredient. Afterwards each unit is infected with 10-20 larvae of the banded cucumber beetle (Diabrotica balteata). After 7 days efficacy in % is determined. 100 % means all the seedlings have grown up like in the untreated, uninfected control; 0 % means none of the seedlings have grown.
  • the plates are sealed with parafilm through which a mixed population of the green peach aphid (Myzus persicae) can suck on the compound preparation.
  • mortality in % is determined.100 % means all aphids have been killed and 0 % means none of the aphids have been killed.
  • the following compounds from the preparation examples showed good activity of 100 % at an application rate of 4 ppm: I-34.
  • the following compounds from the preparation examples showed good activity of 90 % at an application rate of 4 ppm: I-20.
  • the following compounds from the preparation examples showed good activity of 100 % at an application rate of 0.8 ppm: I-8.
  • Nezara viridula – spray test Solvent: 78.0 parts by weight of acetone 1.5 parts by weight of dimethylformamide
  • Emulsifier alkylarylpolyglycol ether
  • To produce a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water.
  • Rice plants (Oryza sativa) are sprayed with a preparation of the active ingredient of the desired concentration and the plants are infested with the brown planthopper (Nilaparvata lugens). After 4 days mortality in % is determined.100 % means all planthoppers have been killed and 0 % means none of the planthoppers have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 500 g/ha: I-83, I-85, I-132, I-134, I-140, I-141. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 g/ha: I-8.
  • Spodoptera frugiperda – spray test Solvent: 78.0 parts by weight acetone 1.5 parts by weight dimethylformamide
  • Emulsifier alkylarylpolyglycol ether
  • To produce a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvents and is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water.
  • Maize (Zea mays) leaf sections are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf sections are infested with fall armyworm larvae (Spodoptera frugiperda).
  • This solution is pipetted onto a glazed tile and after evaporation of the acetone, adult mosquitoes of the species Aedes aegypti strain MONHEIM are placed onto the dried surface. The exposure time is 30 minutes. Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died.
  • the following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m 2 : I-7, I-8, I-9, I-10, I-85.
  • the following examples showed in this test efficacy of 80-100% at a surface concentration of 4 mg/m 2 : I- 7, I-8, I-9, I-10.
  • Anopheles funestus test (ANPHFU surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME)
  • RME rapeseed oil methyl ester
  • Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died.
  • the following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m 2 : I-7, I-8, I-9, I-10, I-85.
  • the following examples showed in this test efficacy of 80-100% at a surface concentration of 4 mg/m 2 : I- 9.
  • Musca domestica test (MUSCDO surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME)
  • RME rapeseed oil methyl ester

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Abstract

The present invention relates to novel heteroaryl-substituted pyrazine derivatives of the general formula (I), in which the structural elements R1, R2, R3, R4, R5 and R6 have the meaning given in the description, to formulations and compositions comprising such compounds and for their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.

Description

HETEROARYL-SUBSTITUTED PYRAZINE DERIVATIVES AS PESTICIDES
The present invention relates to novel heteroaryl-substituted pyrazine derivatives, to formulations and compositions comprising such compounds and to their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.
Certain heteroaryl-triazole and heteroaryl-tetrazole compounds are disclosed for the use in controlling of ectoparasites on animals in WO 2017/192385 and for the use in controlling of animal pests in the field of plant protection in WO 2019/170626 and WO 2019/215198.
Further, the patent applications WO 2019/201835 (PCT/EP 2019/059624), WO 2019/197468 (PCT/EP 2019/059089), WO 2019/202077 (PCT/EP 2019/060081), WO 2019/206799 (PCT/EP 2019/060077), EP 19169209.4, EP 19187891.7, and EP 19187899.0 (the latter three not yet published) relate to triazole - and tetrazole-compoundsand their use in crop protection and/or their use as pesticides.
WO 2020/002563, WO 2020/053364, WO 2020/053365, WO 2020/079198 and WO 2020/169445 describe azole-amide compounds whereas WO 2020/070049 relates to pyrazine compounds all of which can be used as insecticides.
Modern plant protection products and veterinary ectoparasiticides have to meet many demands, for example in relation to efficacy, persistence, spectrum and resistance breaking properties. Questions of toxicity, the combinability with other active compounds or formulation auxiliaries play a role, as well as the question of the expense that the synthesis of an active compound requires. Furthermore, resistances may occur. Resistant parasites are an icreasing problem both for farm animals as well as for companion animals and also in crop pests. For all these reasons, the search for novel crop protection compositions or veterinary ectoparasiticides cannot be considered to be complete, and there is a constant need for novel compounds having properties which, compared to the known compounds, are improved at least in respect of individual aspects. It is in particular desirable to find new pesticides and parasiticides that overcome resistance.
It was an object of the present invention to provide compounds which widen the spectrum of the pesticides in various aspects.
Therefore, in a first aspect (aspect 1.1) the invention relates to compounds of the general formula (I)
Figure imgf000003_0001
in which R1 is hydrogen; in each case optionally substituted C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6haloalkynyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl; or heterocyclyl-C1-C6alkyl, wherein the heterocyclyl is selected from the group consisting of saturated and partially unsaturated 3- to 10-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, 9-membered heteroaryl and 10-membered heteroaryl and the heterocyclyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3halo- alkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl R2 is phenyl or a 5- or 6-membered heteroaryl, each of which is optionally substituted with 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C6haloalkyl, C1-C6alkoxy, C3-C6cycloalkoxy, C1-C6haloalkoxy, hydroxy-C1-C6alkyl, -CO2C1-C6alkyl, -NH(C1-C6alkyl), -N(C1-C6alkyl)2, S-C1- C6alkylsulfinimidoyl, S-C3-C6cycloalkylsulfinimidoyl, S-C2-C6alkenylsulfinimidoyl, S- C2-C6alkinylsulfinimidoyl, S-phenylsulfinimidoyl, S-heterocyclylsulfinimidoyl, S- heteroarylsulfinimidoyl, S-C1-C6alkylsulfonimidoyl, S-C3-C6cycloalkylsulfonimidoyl, S-C2-C6alkenylsulfonimidoyl, S-C2-C6alkinylsulfonimidoyl, S-phenylsulfonimidoyl, S- heterocyclylsulfonimidoyl, S-heteroarylsulfonimidoyl, -C(=NOC1-C6alkyl)H, - C(=NOC1-C6alkyl)-C1-C6alkyl, (C1-C6alkyl)3-silyl; - and the substructures S1 – S9, in which the bond to the phenyl or 5- or 6-membered heteroaryl is marked with a # and Z is CO or CS and Y is independently selected from CO or SO2;
Figure imgf000004_0001
R21 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, C3-C6cycloalkyl, -C1-C6alkyl-C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; R22 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, -C1-C6alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R23 is independently selected from in each case optionally substituted C1- C6alkyl, C1-C6haloalkyl, C3-C6cycloalkyl and phenyl; R24 is in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C6haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; or R21 and R22 together with the nitrogen atom to which they are attached, represent a monocyclic or polycyclic optionally substituted 3- to 12-membered saturated or unsaturated heterocyclyl which may contain further heteroatoms; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1- C6alkyl, C3-C6cycloalkyl, C3-C6cycanocycloalkyl, C3-C6halocycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C6cyanocycloalkyl, C1- C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R3 is hydrogen or C1-C6alkyl optionally substituted with 1 to 3 substituents selected from halogen, C3-C6-cycloalkyl and C1-C6-alkoxy; R4 is a monocyclic heterocycle selected from the group consisting of a 5-membered heteroaryl, a 6-membered heteroaryl and a 3-6 membered heterocyclyl, each of which containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, and each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C6alkyl-C3-C6cycloalkyl, C1-C6haloalkyl, C3-C6halocycloalkyl, C1- C6alkoxy, C3-C6cycloalkoxy, C1-C6haloalkoxy, hydroxy-C1-C6alkyl, -NH(C1-C6alkyl), - NH(C1-C6alkyl-C3-C6cycloalkyl), -N(C1-C6alkyl)2, -N(C1-C6alkyl)(C1-C6alkyl-C3- C6cycloalkyl), -CO2C1-C6alkyl, S-C1-C6alkylsulfinimidoyl, S-C3- C6cycloalkylsulfinimidoyl, S-C2-C6alkenylsulfinimidoyl, S-C2-C6alkinylsulfinimidoyl, S-phenylsulfinimidoyl, S-heterocyclylsulfinimidoyl, S-heteroarylsulfinimidoyl, S-C1- C6alkylsulfonimidoyl, S-C3-C6cycloalkylsulfonimidoyl, S-C2-C6alkenylsulfonimidoyl, S-C2-C6alkinylsulfonimidoyl, S-phenylsulfonimidoyl, S-heterocyclylsulfonimidoyl, S- heteroarylsulfonimidoyl, -C(=NOC1-C6alkyl)H, -C(=NOC1-C6alkyl)-C1-C6alkyl; - and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1- C6alkyl, C3-C6cycloalkyl, C3-C6cycanocycloalkyl, C3-C6halocycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1- C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; - and the following substructures S10 – S18, in which the bond to the pyrazine is marked with a # and Z is CO or CS and Y is independently selected from CO or SO2:
Figure imgf000007_0001
R41 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, C3-C6cycloalkyl, -C1-C6alkyl-C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; R42 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl and C3-C6cycloalkyl; R43 is independently selected from in each case optionally substituted C1- C6alkyl, C1-C6haloalkyl, C3-C6cycloalkyl and phenyl; R44 is in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C6haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a monocyclic or polycyclic optionally substituted 3- to 12-membered saturated or unsaturated heterocyclyl which may contain further heteroatoms; R5 is hydrogen, halogen, -CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4-cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1- C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, -NH2, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl; R6 is hydrogen, halogen, -CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, -CO2(C1- C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1- C4alkyl)-C1-C4alkyl, -NH2, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3- C6cycloalkylsulfonyl; and salts and N-oxides thereof. The compounds of the formula (I) described anywhere herein likewise encompass any diastereomers or enantiomers and E/Z isomers which exist, and also salts and N-oxides of compounds of the formula (I). The compounds of the formula (I) described anywhere herein may possibly also, depending on the nature of the substituents, be in the form of stereoisomers, i.e. in the form of geometric and/or optical isomers or isomer mixtures of varying composition. This invention provides both the pure stereoisomers and any desired mixtures of these isomers, even though it is generally only compounds of the formula (I) that are discussed here. However, preference is given in accordance with the invention to using the optically active, stereoisomeric forms of the compounds of the formula (I) and salts thereof. The invention therefore relates both to the pure enantiomers and diastereomers and to mixtures thereof. According to an embodiment of the present invention dextrorotatory compounds of formula (I) are preferred, i.e. those isomers which rotate plane-polarized light clockwise ((+)-direction). Such enantiomers are usually designated with “(+)“. Methods of separating enantiomers are well-known in the art, e.g. separation via chiral chromatography. At the carbon atom in formula (I) which carries R3 the present cocompounds can have R- or S- configuration (according to the Cahn-Ingold-Prelog rules). The present invention relates to compounds which have R- or S-configuration at this site as well as to mixtures of these isomers. According to a further embodiment compounds of formula (I) are preferred which have an S-configuration at the carbon atom which carries R3. If appropriate, the compounds of the formula (I) may be present in various polymorphic forms or as a mixture of various polymorphic forms. Both the pure polymorphs and the polymorph mixtures are provided by the invention and can be used in accordance with the invention. The invention further relates to preferred embodiments as defined in the following aspects of the invention: According to the following embodiments compounds of the formula (I) are excluded from the present invention: (i) According to a one embodiment compounds of formula (I) are excluded, wherein R2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein the phenyl, pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1-C3thiohaloalkyl, C1-C3alkoxy, C1- C3haloalkoxy, halogen, NO2, SF5, CN, CONH2, COOH and C(S)NH2. (ii) According to a further embodiment compounds of formula (I) are excluded, wherein R2 is phenyl or pyridine wherein the phenyl or pyridine is optionally substituted with one or two substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1-C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, and -CN; or wherein preferably each substituent is selected from: C1-C3alkyl, C1-C3haloalkyl, C1- C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, and halogen. (iii) According to a further embodiment compounds of formula (I) are excluded, wherein R4 is pyridine, pyrimidine, pyrazine or pyridazine wherein the pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, independently selected, from C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C3-C4cycloalkyl, halogen and hydroxy. (iv) According to a further embodiment compounds of formula (I) are excluded, wherein R4 is pyridine or pyrimidine wherein the pyridine or pyrimidine is optionally substituted with one substituent selected from C1-C3alkyl, C3-C4cycloalkyl or halogen or hydroxy; or wherein preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from,C3-C4cycloalkyl or halogen and hydroxy; or wherein more preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from C3-C4cycloalkyl, F, Cl and Br. (v) According to a further embodiment compounds of formula (I) are excluded, wherein R2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein the phenyl, pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1-C3thiohaloalkyl, C1-C3alkoxy, C1- C3haloalkoxy, halogen, NO2, SF5, CN, CONH2, COOH and C(S)NH2, and at the same time R4 is pyridine, pyrimidine, pyrazine or pyridazine wherein the pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, independently selected, from C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C3-C4cycloalkyl, halogen or hydroxy. (vi) According to a further embodiment compounds of formula (I) are excluded wherein R2 is phenyl, pyridine, pyrimidine, pyrazine or pyridazine, wherein the phenyl, pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1-C3thiohaloalkyl, C1-C3alkoxy, C1- C3haloalkoxy, halogen, NO2, SF5, CN, CONH2, COOH and C(S)NH2; and at the same time R4 is pyridine or pyrimidine wherein the pyridine or pyrimidine is optionally substituted with one substituent selected from C1-C3alkyl, C3-C4cycloalkyl or halogen or hydroxy; or wherein preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from,C3-C4cycloalkyl or halogen and hydroxy; or wherein more preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from C3-C4cycloalkyl, F, Cl and Br. (vii) According to a further embodiment compounds of formula (I) are excluded wherein R2 is phenyl or pyridine wherein the phenyl or pyridine is optionally substituted with one or two substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1- C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, and -CN; or wherein preferably each substituent is selected from: C1-C3alkyl, C1-C3haloalkyl, C1- C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, and halogen; and at the same time R4 is pyridine, pyrimidine, pyrazine or pyridazine wherein the pyridine, pyrimidine, pyrazine or pyridazine is optionally substituted with one to three substituents, independently selected, from C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C3-C4cycloalkyl, halogen or hydroxy. (viii) According to a further embodiment compounds of formula (I) are excluded wherein R2 is phenyl or pyridine wherein the phenyl or pyridine is optionally substituted with one or two substituents, provided the substituent(s) are not on either carbon adjacent to the carbon C=O is attached, and each substituent is independently selected from: C1-C3alkyl, C1-C3haloalkyl, C1- C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, halogen, and -CN; or wherein preferably each substituent is selected from: C1-C3alkyl, C1-C3haloalkyl, C1- C3thiohaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, and halogen; and at the same time R4 is pyridine or pyrimidine wherein the pyridine or pyrimidine is optionally substituted with one substituent selected from C1-C3alkyl, C3-C4cycloalkyl or halogen or hydroxy; or wherein preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from,C3-C4cycloalkyl or halogen and hydroxy; or wherein more preferably the pyridine or pyrimidine is optionally substituted with one substituent selected from C3-C4cycloalkyl, F, Cl and Br. In a further aspect (aspect 1.2) the invention relates to compounds of the general formula (I)
Figure imgf000011_0001
in which R1 is hydrogen; in each case optionally substituted C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C3alkoxyC1-C3alkyl, C1- C3alkylthioC1-C3alkyl, C1-C3alkylsulfinylC1-C3alkyl, C1-C3alkylsulfonylC1-C3alkyl, C1- C3haloalkyl, C1-C6cyanoalkyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1- C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1- C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R2 is phenyl or a 5- or 6-membered heteroaryl, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, CN, - COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C3- C6cycloalkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3- C6cycloalkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl, alkenylthio, alkynylthio, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -NHCO-C1-C4alkyl, NHCO-C3- C6cycloalkyl, -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3- C6cycloalkyl, -N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH-phenyl, -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, (C1-C4alkyl)3-silyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl, and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1- C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; is hydrogen or optionally substituted C1-C6alkyl; R4 is a monocyclic heterocycle selected from the group consisting of a 5-membered heteroaryl, a 6-membered heteroaryl and a 3-6 membered heterocyclyl, each of which containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, and each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl, C1-C4alkyl-C3-C6cycloalkyl, C1- C3haloalkyl, C1-C3cyanoalkyl, C3-C6halocycloalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C3-C6cycloalkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1- C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylthio, C3- C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl, alkenylthio, alkynylthio, -NH(C1-C4alkyl), -NH(C1-C4alkyl-C3- C6cycloalkyl), -N(C1-C4alkyl)2, -N(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -NHCO-C1- C4alkyl, NHCO-C3-C6cycloalkyl, -NHCO(C1-C4alkyl-C3-C6cycloalkyl), -NHSO2(C1- C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3-C6cyclolkyl, -N(C1- C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH(C1-C4alkyl-C3-C6cycloalkyl), -CONH-phenyl, -CONHSO2(C1-C4alkyl), -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -CON(C1- C4alkyl)SO2(C1-C4alkyl), -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1- C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1- C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R5 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4-cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -C(O)-C1-C3alkoxy, -CH-(C1- C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, NH2, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3alkylthio, C3-C6cycloalkylthio; R6 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, -C(O)-C1- C3alkoxy, -CH-(C1-C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1- C4alkyl)-C1-C4alkyl, NH2, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3alkylthio, C3- C6cycloalkylthio; and salts and N-oxides thereof. In a further aspect (aspect 2.1) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C6alkoxyC1-C6alkyl, C1-C6alkylthioC1-C6alkyl, C1- C6alkylsulfinylC1-C6alkyl, C1-C6alkylsulfonylC1-C6alkyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C6alkyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cyano- cycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl; or heterocyclyl-C1-C3alkyl, wherein the heterocyclyl is selected from the group consisting of tetrahydropyranyl, tetrahydrofuranyl, oxetanyl and azetidinyl, or heteroaryl, wherein the heteroaryl is selected from the group consisting of pyridyl, pyrimidinyl, pyrazyl, pyridazinyl, thiophenyl, furanyl, pyrazolyl, imidazolyl, triazolyl, thiazolyl, and oxazolyl, and wherein the heteroaryl or the heterocyclyl is optionally substituted with 1 to 3 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, - CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycano- cycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3halo- alkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole and thiophene, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C4alkoxy, C3-C6cycloalkoxy, C1-C3haloalkoxy, hydroxy-C1-C4alkyl, -CO2C1-C4alkyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -C(=NOC1- C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl and (C1-C4alkyl)3-silyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; - and the substructures S1, S4, S7, S8 and S9, in which the bond to the aforementioned phenyl, pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole or thiophene is marked with a # and Z is CO or CS; -
Figure imgf000015_0001
R21 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, C3-C6cycloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and 3- to 6-membered heterocyclyl; R22 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R24 is in each case optionally substituted C1-C4alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C4haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and 3- to 6-membered heterocyclyl; wherein the aforementioned optionally substituted radicals in the definitions of R21, R22 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1- C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; or R21 and R22 together with the nitrogen atom to which they are attached, represent a 4- to 12-membered saturated or unsaturated heterocyclyl which may contain up to two further heteroatoms selected from the group of oxygen, nitrogen and sulfur and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, -SF5, and -NH2; and C1-C4alkyl, C3-C6cycloalkyl, C1-C4haloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C3- C6cycloalkylsulfanyl, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1- C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl; R3 is hydrogen or C1-C6alkyl optionally substituted with halogen, cyano, C3-C6cycloalkyl or C1- C4alkoxy; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine, and thiazole, pyrazole, pyrrole, oxazole, isothiazole, isoxazole, thiophene and imidazole, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C4alkoxy, C3-C6cycloalkoxy, C1-C3haloalkoxy, hydroxy-C1-C4alkyl, -CO2C1-C4alkyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -C(=NOC1- C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl and (C1-C4alkyl)3-silyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C3alkylsulfonyl, C3- C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; - and the substructures S10, S11, S13, S14, S16, S17 and S18, in which the bond to the aforementioned pyridine, pyrimidine, pyrazine, pyridazine, thiazole, pyrazole, pyrrole, oxazole, isothiazole, isoxazole, thiophene or imidazole is marked with a # and Z is CO or CS;
Figure imgf000017_0001
R41 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, C3-C6cycloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and 3- to 6-membered heterocyclyl; R42 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R43 is independently selected from in each case optionally substituted C1- C4alkyl, C1-C4haloalkyl and C3-C6cycloalkyl; R44 is in each case optionally substituted C1-C4alkyl, C1-C4haloalkyl, C3- C6cycloalkyl, phenyl, heteroaryl and 3- to 6-membered heterocyclyl; wherein the aforementioned optionally substituted radicals in the definitions of R41, R42, R43 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a 4- to 12-membered saturated or unsaturated heterocyclyl which may contain up to two further heteroatoms selected from the group of oxygen, nitrogen, sulfur and silicon and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, -SF5, and -NH2; and C1-C4alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkoxy-C1-C6alkyl, C1-C4alkylthio, C1- C4alkylsulfinyl, C1-C4alkylsulfonyl, C3-C6cycloalkylsulfanyl, C3- C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1-C4haloalkylthio, C1- C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl; R5 is hydrogen, halogen, -CN, -NH2, or in each case optionally substituted C1-C3-alkyl, C3-C4- cycloalkyl, C1-C3alkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), - CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1- C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3- alkylthio, C3-C6cycloalkylthio, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C3alkyl; R6 is hydrogen, halogen, -CN, -NH2, or in each case optionally substituted C1-C3-alkyl, C3-C4- cycloalkyl, C1-C3alkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), - CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1- C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3- alkylthio, C3-C6cycloalkylthio, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C3alkyl; and salts and N-oxides thereof. In a further aspect (aspect 2.2) the invention relates to compounds or the formula (I) as described supra, in which R1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3haloalkyl, C1-C6cyanoalkyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1- C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1- C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene and imidazole, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C1- C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -NHCO-C1-C4alkyl, NHCO-C3- C6cycloalkyl, -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3- C6cyclolkyl, -N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, - CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH-phenyl, -CON(C1-C4alkyl)2, - CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -C(=NOC1-C4alkyl)H, - C(=NOC1-C4alkyl)-C1-C4alkyl, (C1-C4alkyl)3-silyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl, and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl; R3 is hydrogen or optionally substituted C1-C6alkyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine and thiazole, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C3-C6cycloalkyl, C1-C4alkyl-C3-C6cycloalkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C3-C6halocycloalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1- C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1- C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl, -NH(C1-C4alkyl), -NH(C1-C4alkyl-C3- C6cycloalkyl), -N(C1-C4alkyl)2, -N(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -NHCO-C1- C4alkyl, NHCO-C3-C6cycloalkyl, -NHCO(C1-C4alkyl-C3-C6cycloalkyl), -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3-C6cyclolkyl, -N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH(C1-C4alkyl-C3-C6cycloalkyl), -CONH-phenyl, -CONHSO2(C1-C4alkyl), -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -CON(C1- C4alkyl)SO2(C1-C4alkyl), -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1- C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1- C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1- C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R5 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4-cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -C(O)-C1-C3alkoxy, -CH-(C1- C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, NH2, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3alkylthio, C3-C6cycloalkylthio; R6 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -C(O)-C1-C3alkoxy, -CH-(C1- C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, NH2, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3alkylthio, C3-C6cycloalkylthio; and salts and N-oxides thereof. In a further aspect (aspect 3.1) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; or C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2- C6alkynyl, C2-C6haloalkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3alkylsulfinylC1-C3alkyl, C1-C3alkylsulfonylC1-C3alkyl, C1-C6haloalkyl, C1-C6cyanoalkyl; R2 is selected from the group consisting of pyrazole, phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by a total of 1, 2 or 3 substituents, wherein 1, 2 or 3 of the optional substituents are independently selected from group A consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C4alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C3-C4cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C3- C4cycloalkoxy, C1-C3cyanoalkoxy, -CO2C1-C4alkyl and (C1-C3alkyl)3-silyl; and optionally 1 of the optional substituents may be selected from group B consisting of - the substructures S1, S4, S7, S8 and S9, in which the bond to the phenyl, pyridine, pyrimidine, pyrazine, or pyridazine is marked with a # and Z is CO;
Figure imgf000022_0001
R21 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl; R22 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl and C3-C4cycloalkyl; R24 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl and phenyl; wherein the aforementioned optionally substituted radicals in the definitions of R21, R22 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1- C3haloalkyl; R3 is hydrogen or C1-C6alkyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene and imidazole, wherein the aforementioned 6-membered heteroaryl are each optionally substituted by 1, 2 or 3 substituents and the aforementioned 5-membered heteroaryl are each optionally substituted by 1 or 2 substituents, wherein in each case up to all of the optional substituents are independently selected from group D consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3- C4cyanocycloalkyl, C1-C3alkoxy, C3-C4cycloalkoxy, C1-C3haloalkoxy, C1- C3cyanoalkoxy, hydroxy-C1-C3alkyl, -CO2C1-C3alkyl, -NH(C1-C3alkyl), -N(C1- C3alkyl)2, -C(=NOC1-C3alkyl)H, -C(=NOC1-C3alkyl)-C1-C3alkyl and (C1-C3alkyl)3- silyl; and optionally 1 of the optional substituents may be selected from group E consisting of - the substructures S10, S13, S16, S17 and S18, in which the bond to the aforementioned pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene or imidazole is marked with a # and Z is CO;
Figure imgf000023_0001
R41 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and 3- to 6-membered heterocyclyl containing 1 heteroatoms selected from the group consisting of N, O, and S; R42 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and C3-C4cycloalkyl; R44 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl; wherein the aforementioned optionally substituted radicals defined for R41, R42 and R44 are optionally substituted with up to 2 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1-C3haloalkyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a monocyclic 4- to 8-membered saturated heterocyclyl which may contain up to one further heteroatom selected from the group of oxygen, nitrogen, sulfur and silicon and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, and -NH2; and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R5 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4-cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R6 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; and salts and N-oxides thereof. In a further aspect (aspect 3.2) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; or C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2- C6alkynyl, C2-C6haloalkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3alkylsulfinylC1-C3alkyl, C1-C3alkylsulfonylC1-C3alkyl, C1-C6haloalkyl, C1-C6cyanoalkyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by a total of 1, 2 or 3 substituents, wherein 1, 2 or 3 of the optional substituents are independently selected from group A consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C4alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C3-C4cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C3- C4cycloalkoxy, C1-C3cyanoalkoxy, -CO2C1-C4alkyl and (C1-C3alkyl)3-silyl; and optionally 1 of the optional substituents may be selected from group B consisting of - the substructures S1, S4, S7, S8 and S9, in which the bond to the phenyl, pyridine, pyrimidine, pyrazine, or pyridazine is marked with a # and Z is CO;
Figure imgf000025_0001
R21 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl; R22 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl and C3-C4cycloalkyl; R24 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl and phenyl; wherein the aforementioned optionally substituted radicals in the definitions of R21, R22 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1- C3haloalkyl; R3 is hydrogen or C1-C6alkyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene and imidazole, wherein the aforementioned 6-membered heteroaryl are each optionally substituted by 1, 2 or 3 substituents and the aforementioned 5-membered heteroaryl are each optionally substituted by 1 or 2 substituents, wherein in each case up to all of the optional substituents are independently selected from group D consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3- C4cyanocycloalkyl, C1-C3alkoxy, C3-C4cycloalkoxy, C1-C3haloalkoxy, C1- C3cyanoalkoxy, hydroxy-C1-C3alkyl, -CO2C1-C3alkyl, -NH(C1-C3alkyl), -N(C1- C3alkyl)2, -C(=NOC1-C3alkyl)H, -C(=NOC1-C3alkyl)-C1-C3alkyl and (C1-C3alkyl)3- silyl; and optionally 1 of the optional substituents may be selected from group E consisting of - the substructures S10, S13, S16, S17 and S18, in which the bond to the aforementioned pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene or imidazole is marked with a # and Z is CO;
Figure imgf000026_0001
R41 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and 3- to 6-membered heterocyclyl containing 1 heteroatoms selected from the group consisting of N, O, and S; R42 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and C3-C4cycloalkyl; R44 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl. wherein the aforementioned optionally substituted radicals defined for R41, R42 and R44 are optionally substituted with up to 2 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1-C3haloalkyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a monocyclic 4- to 8-membered saturated heterocyclyl which may contain up to one further heteroatom selected from the group of oxygen, nitrogen, sulfur and silicon and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, and -NH2; and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R5 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4-cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R6 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; and salts and N-oxides thereof. In a further aspect (aspect 3.3) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C6cyanoalkyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3- C6cyanocycloalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylthio, C3- C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -NHCO-C1-C4alkyl, NHCO-C3- C6cycloalkyl, -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3- C6cyclolkyl, -N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH-phenyl, -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, (C1-C4alkyl)3-silyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl, and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, C1-C6alkyl and C1-C3cyanoalkyl,; R3 is hydrogen or optionally substituted C1-C6alkyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine and thiazole, each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, C1-C6alkyl, C3-C6cycloalkyl, C1-C4alkyl-C3-C6cycloalkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C3-C6halocycloalkyl, C3-C6cyanocycloalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1- C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, -NH(C1-C4alkyl), -NH(C1- C4alkyl-C3-C6cycloalkyl), -N(C1-C4alkyl)2, -N(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -NHCO-C1-C4alkyl, NHCO-C3-C6cycloalkyl, -NHCO(C1-C4alkyl-C3-C6cycloalkyl), -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3-C6cyclolkyl, -N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH(C1-C4alkyl-C3-C6cycloalkyl), -CONH-phenyl, -CONHSO2(C1-C4alkyl), -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)(C1-C4alkyl-C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -CON(C1- C4alkyl)SO2(C1-C4alkyl), -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, -SO2NH2, -SO2NH(C1-C4alkyl), phenylsulfonyl and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, C1-C6alkyl and C1-C3cyanoalkyl; R5 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4-cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -C(O)-C1-C3alkoxy, -CH-(C1- C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl; R6 is hydrogen, halogen, CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -C(O)-C1-C3alkoxy, -CH-(C1- C3alkoxy)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl; and salts and N-oxides thereof. In a further aspect (aspect 4.1) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, methylsulfonylethyl, ethylsulfonylethyl; R2 is selected from the group consisting of pyrazole, phenyl and pyridine each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, 1-cyano-1-methyleth-1-yl,, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl, phenylsulfonyl which may carry a fluorine, chlorine or methyl substituent; R3 is hydrogen, methyl, ethyl, n-propyl, or isopropyl; R4 is selected from the group consisting of pyridin-2-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H- pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, -COOH, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, cyclobutyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, -COOCH3, - COOCH2CH3, and the substructures S13, in which the bond to the aforementioned pyridin-2-yl, pyrimidin- 2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H-pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, is marked with a # and Z is CO;
Figure imgf000030_0001
R41 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R42 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, azepane, morpholine, oxazepane, azasilolidine, azasilinane, azasilepane each of which is optionally substituted with 1 or 2 methyl groups; R5 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; R6 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; and salts and N-oxides thereof. In a further aspect (aspect 4.2) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, methylsulfonylethyl, ethylsulfonylethyl; R2 is selected from the group consisting of phenyl and pyridine each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, 1-cyano-1-methyleth-1-yl (also referred to as 1-methyl-1- cyanoethyl), methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl, phenylsulfonyl which may carry a fluorine, chlorine or methyl substituent; R3 is hydrogen, methyl, ethyl, n-propyl, or isopropyl; R4 is selected from the group consisting of pyridin-2-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H- pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, -COOH, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, cyclobutyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, -COOCH3, - COOCH2CH3, and the substructures S13, in which the bond to the aforementioned pyridin-2-yl, pyrimidin- 2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H-pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, is marked with a # and Z is CO;
Figure imgf000032_0001
R41 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R42 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, azepane, morpholine, oxazepane, azasilolidine, azasilinane, azasilepane each of which is optionally substituted with 1 or 2 methyl groups R5 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; R6 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; and salts and N-oxides thereof. In a further aspect (aspect 4.3) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, isopropan-2-ol, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl, -SO2NH2, phenylsulfonyl which may carry a fluorine, chlorine or methyl substituent, and oxetane , tetrahydropyrane and piperazine which each may carry a methyl substituent; R3 is hydrogen, methyl, ethyl, n-propyl, or isopropyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine and thiazole, each of which is optionally substituted by 1, 2, or 3 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, CN, -COOH, -CONH2, -NO2, -NH2, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, isopropan-2-ol, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, -NH(CH3), -N(CH3)2, -NHCO-CH3, NHCO-cyclopropyl, -CON(CH3)(CH3-cyclopropyl), , -SO2NH2, and phenylsulfonyl which may carry a fluorine, chlorine, methyl or cyanomethyl substituent; R5 is hydrogen, fluorine, chlorine, bromine, iodine, CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; R6 is hydrogen, fluorine, chlorine, bromine, iodine, CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; and salts and N-oxides thereof. In a further aspect (aspect 5.1) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen, or cyclopropylmethyl; R2 is selected from the group consisting of pyrazol, phenyl and pyridine, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, tert- butyl, 1-cyano-1-methyleth-1-yl, cyclopropyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, 4- fluorophenylsulfonyl, difluoromethylsulfonyl; R3 is methyl; R4 is selected from the group consisting of pyridine-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl, 1H- pyrazol-1-yl each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH3, -COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the C-5-position of the aforementioned pyridin-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl -, or to the C-4-position in the above mentioned 1H-pyrazol- 1-yl, and Z is CO;
Figure imgf000035_0001
S13 R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl, cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, or (Si,Si- dimethyl)azasilinane; R5 is hydrogen or methyl; R6 is hydrogen or methyl; and salts and N-oxides thereof. In a further aspect (aspect 5.2) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen, or cyclopropylmethyl; R2 is selected from the group consisting of phenyl and pyridine, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, tert-butyl, cyclopropyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl; R3 is methyl; R4 is selected from the group consisting of pyridine-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl, 1H- pyrazol-1-yl each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH3, -COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the C-5-position of the aforementioned pyridin-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl -, or to the C-4-position in the above mentioned 1H-pyrazol- 1-yl, and Z is CO;
Figure imgf000036_0001
S13 R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, (Si,Si- dimethyl)azasilinane, R5 is hydrogen or methyl; R6 is hydrogen or methyl; and salts and N-oxides thereof. In a further aspect (aspect 5.3) the invention relates to compounds of the formula (I) as described supra, in which R1 is hydrogen, methyl, cyclopropylmethyl, ethoxymethyl or ethylthiomethyl; R2 is selected from the group consisting of phenyl and pyridine, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of fluorine, chlorine, bromine, CN, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, trifluoromethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, isopropan-2-ol, (CH3)3-silyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, -SO2NH2, phenylsulfonyl which may carry a fluorine substituent, and oxetane, tetrahydropyrane and piperazine which each may carry a methyl substituent; R3 is methyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine and thiazole, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, trifluoromethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, isopropan-2-ol, -NHCO-CH3, NHCO-cyclopropyl, -CON(CH3)(CH3-cyclopropyl), and methylsulfonyl; R5 is hydrogen, fluorine, chlorine, bromine, iodine, CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, or trifluoromethoxy; R6 is hydrogen, fluorine, chlorine, bromine, iodine, CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, or trifluoromethoxy; and salts and N-oxides thereof. In a further aspect (aspect 6) the invention relates to compounds of the formula (I) as described supra, in which R2 is phenyl which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof. In one preferred embodiment of aspect 6 of the invention supra R2 is the following substructure Q1, in which the bond to the C=O-group is marked with a #:
Figure imgf000038_0001
wherein R25 is hydroxy, -NH2, -SO2NH2, C4-C6alkyl, C4alkoxy, C1-C3cyanoalkyl, C3-C6cycloalkyl, C3- C6halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C3-C6cycloalkylsulfanyl, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, - NH(C1-C4alkyl), -N(C1-C4alkyl)2, -NHCO-C1-C4alkyl, NHCO-C3-C6cycloalkyl, - NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3-C6cyclolkyl, - N(C1-C4alkyl)SO2C1-C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), -CONH-phenyl, -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)-phenyl, -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, (C1-C4alkyl)3-silyl, -SO2NH(C1-C4alkyl), phenylsulfonyl, or 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the aforementioned substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, CN, C1-C6alkyl, C1-C6haloalkyl and C1-C3cyanoalkyl; and R26 is halogen, -CN, -COOH, -CONH2, -NO2, -SF5, C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3haloalkylthio, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3- alkylsulfonyl, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C3-C6cycloalkylsulfanyl, C3- C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C3-C6cycloalkyl, C1-C3cyanoalkyl, C3- C6cyanocycloalkyl. R25 and R26 are preferably defined as follows: R25 is -SO2NH2, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl, cyanomethoxy, tert-butyl, cyclopropyl, cyanomethyl, 1-cyano-1-methyleth-1-yl, 1-cyanocyclopropyl, isopropan-2-ol, phenylsulfonyl which may optionally carry a fluorine substituent; or is oxetane, tetrahydropyrane or piperazine which each may optionally carry a methyl substituent; R26 is fluorine, chlorine, bromine, CN, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, difluorormethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl. According to a further embodiment R25 and R26 are preferably defined as follows: R25 is -SO2NH2, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl, cyanomethoxy, tert-butyl, cyclopropyl, cyanomethyl, isopropan-2-ol, phenylsulfonyl which may optionally carry a fluorine substituent; or is oxetane, tetrahydropyrane or piperazine which each may optionally carry a methyl substituent; R26 is fluorine, chlorine, bromine, CN, SF5, methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl. R25 and R26 are particularly preferably defined as follows: R25 is methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, tert-butyl, cyclopropyl, 1-cyano-1-methyleth-1-yl,1-cyanocyclopropyl, 4-fluorophenylsulfonyl; and R26 is fluorine, chlorine, bromine, iodine, CN, SF5, methyl, ethyl, isopropyl, tert.-butyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl. According to a further embodiment R25 and R26 are particularly preferably defined as follows: R25 is methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, tert-butyl, cyclopropyl; and R26 is fluorine, chlorine, bromine, CN, SF5, methyl, ethyl, isopropyl, tert.-butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, cyclopropyl. In further embodiment of aspect 6 of the invention supra R2 is the following substructure Q2, in which the bond to the C=O-group is marked with a # and
Figure imgf000040_0002
wherein R27 is halogen, -CN, -COOH, -CONH2, -NO2, -SF5, C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy or C1-C3haloalkylthio; and R28 is halogen, -CN, -COOH, -CONH2, -NO2, -SF5, C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, or C1-C3haloalkylthio. R27 and R28 are preferably defined as follows: R27 is fluorine, chlorine, bromine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy; R28 is fluorine, chlorine, bromine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy. In a further aspect (aspect 7) the invention relates to compounds of the formula (I) as described supra, in which R2 is thiophene, pyrazole or imidazole, each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof. In a preferred embodiment of aspect 7 of the invention supra R2 is selected from an optionally substituted thiophene and a pyrazole group:
Figure imgf000040_0001
wherein R9 is selected from halogen, preferably fluorine, chlorine and bromine, C1-C3alkyl, preferably methyl, C1- C3haloalkyl, preferably trifluoromethyl, and pentafluorosulfanyl; n is an integer of 0, 1 or 2, preferably 1 or 2; and Y represents hydrogen, C1-C3alkyl, preferably methyl and ethyl, cycloalkyl, preferably cyclopropyl, C1- C3haloalkyl, preferably trifluoromethyl. Preferred examples of such groups R2 are represented by the following formulae:
Figure imgf000041_0001
* * . In a further aspect (aspect 8) the invention relates to compounds of the formula (I) as described supra, in which R4 is selected from the group consisting of pyridine, pyrimidine, thiazole, pyrazol and pyrazine each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N-oxides thereof. In a preferred embodiment of the aspect 8 of the invention supra R4 is selected from the group consisting of pyridine, pyrimidine and thiazole, each of which may be substituted as defined anywhere supra, and wherein the remaining substituents may have the meaning as defined anywhere supra, and salts and N- oxides thereof. In a preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-i), (I-ii) or (I-iii)
Figure imgf000041_0002
wherein R1, R2, R3, R5 and R6 have the meaning as defined in any of the aspects described supra; and R8 represents 0, 1, 2, 3 or 4 same or different substituents as defined in any of the aspects described anywhere supra for R4, preferably R8 represents 0, 1 or 2 substituents, more preferably 0 or 1 substituents; and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-i) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH3(cyclopropylmethyl), CO-N-pyrrolidinyl, CON(CH3(CH2CN); and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-i) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of -CN, -COOH, -COOCH3, - COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the pyridine, preferably in C-5-position, and Z is CO;
Figure imgf000042_0001
R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl or cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, (Si,Si- dimethyl)azasilinane, and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-ii) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH3(cyclopropylmethyl), CO-N-pyrrolidinyl, CON(CH3(CH2CN); and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-ii) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of -CN, -COOH, -COOCH3, - COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the pyrimidine, preferably in C-5-position, and Z is CO;
Figure imgf000043_0001
R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl, or cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, (Si,Si- dimethyl)azasilinane, and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-iii) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH3(cyclopropylmethyl), CO- N-pyrrolidinyl, CON(CH3(CH2CN); and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-iii) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH3, - COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the thiazole, preferably to the C-5-position, and Z is CO;
Figure imgf000044_0002
R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl or cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, (Si,Si- dimethyl)azasilinane, and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-iv)
Figure imgf000044_0001
wherein R1, R2, R3, R5 and R6 have the meaning as defined in any of the aspects described supra; and R8 represents 0, 1, 2 or 3 same or different substituents as defined in any of the aspects described anywhere supra for R4, preferably R8 represents 0, 1 or 2 substituents, more preferably 0 or 1 substituents; and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-iv) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from fluorine, chlorine, bromine, cyano, methyl, trifluormethyl, CONHcyclopropyl, CO-N-morpholinyl, CON(CH3(cyclopropylmethyl), CO- N-pyrrolidinyl, CON(CH3(CH2CN); and salts and N-oxides thereof. In a further preferred embodiment of the aspect 8 of the invention supra the compounds of the formula (I) are characterized by having a structure according to formula (I-iv) supra, and R1, R2, R3, R5, R6 have the meaning as defined in any of the aspects described supra and R8 represents 0, 1 or 2, preferably 0 or 1, 0, 1 or 2, preferably 0 or 1, same or different substituents selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH3, -COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the thiazole, preferably to the C-5-position, and Z is CO;
Figure imgf000045_0001
R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl, cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, (Si,Si- dimethyl)azasilinane, and salts and N-oxides thereof. In a further aspect (aspect 9) the invention relates to compounds of the formula (I) as described in any of the aspects supra, which are characterized by having a structure according to formula (I-v), (I-vi) or (I- vii)
Figure imgf000046_0001
in which R1, R3, R5 and R6 have the meaning as defined in any of the aspects described supra; R7 represents same or different substituents of R2 as defined in any of the aspects described supra; R8 represents same or different substituents of R4 as defined in any of the aspects described supra; n represents an integer of 0, 1 or 2, preferably 0 or 1; m represents an integer of 0, 1 or 2, preferably of 1 or 2; and salts and N-oxides thereof. According to a preferred embodiment of the aspect 9 the invention is directed to compounds of formula (I-v) as defined above. According to a further preferred embodiment of the aspect 9 the invention is directed to compounds of formula (I-vi) as defined above. According to a preferred embodiment of the aspect 9 the invention is directed to compounds of formula (I-vii) as defined above. In a further aspect (aspect 10) the invention relates to compounds of the formula (I) as described in any of the aspects supra, which are characterized by having a structure according to one of the formulae (I-viii), (I-ix), (I-x), (I-xi) and (I-xii)
Figure imgf000047_0001
in which R1, R3, R5 and R6 have the meaning as defined in any of the aspects described supra; R7 represents same or different substituents of R2 as defined in any of the aspects described supra; R8 represents same or different substituents of R4 as defined in any of the aspects described supra; n represents an integer of 0, 1 or 2, preferably 0 or 1; m represents an integer of 0, 1 or 2, preferably of 1 or 2; and salts and N-oxides thereof. According to a preferred embodiment of aspect 10 the invention is directed to compounds of formula (I- viii) as defined above. According to a further preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-ix) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-x) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xi) as defined above. According to a preferred embodiment the aspect 10 of the invention relates to compounds of formulae (I- xii), (I-xiii), (I-xiv), (I-xv), (I-xvi), (I-xvii), (I-xviii) or (I-xix)
Figure imgf000048_0001
Figure imgf000049_0001
in which R1, R3, R5 and R6 have the meaning as defined in any of the aspects described supra; R7 represents same or different substituents of R2 as defined in any of the aspects described supra; R8 represents same or different substituents of R4 as defined in any of the aspects described supra; R81 represents in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, hydroxy-C2-C4alkyl, -CO2C1-C4alkyl, -C(=NOC1-C4alkyl)H, -C(=NOC1- C4alkyl)-C1-C4alkyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, - NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1- C3haloalkylsulfonyl; or represents 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6-membered heterocyclyl may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cyanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl- C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1- C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R81 preferably represents C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3- C4cyanocycloalkyl, , hydroxy-C2-C3alkyl, -CO2C1-C3alkyl, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, - C(=NOC1-C3alkyl)H, or -C(=NOC1-C3alkyl)-C1-C3alkyl; R81 more preferably represents methyl, ethyl, n-propyl, isopropyl, cyclopropyl, cyclobutyl, difluoroethyl, trifluoroethyl, cyanomethyl, cyanoethyl, 2-hydroxyethyl, -COOCH3, or -COOCH2CH3, R81 particularly preferably represents methyl or ethyl, m represents an integer of 0, 1 or 2, preferably of 1 or 2; and salts and N-oxides thereof. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xii) as defined above. According to a further preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xiii) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xiv) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xv) as defined above. According to a further preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xvi) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xvii) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xviii) as defined above. According to a preferred embodiment of the aspect 10 the invention is directed to compounds of formula (I-xix) as defined above. According to one embodiment the invention is directed to compounds of formula (I) as described in the various aspects and embodiments herein, wherein R5 represents hydrogen and the other substituents may have any of the meanings described herein. According to one embodiment the invention is directed to compounds of formula (I) as described in the various aspects and embodiments herein, wherein R6 does not represent hydrogen and the other substituents may have any of the meanings described herein. A further aspect (aspect 11) of the invention relates to the Intermediate Compounds according to formula IX-1, X or XIII wherein R3, R4, R5 and R6 have the meaning as defined in any of the aspects of the invention supra.
Figure imgf000051_0001
Particularly preferred are the compounds according to the Examples infra. Definitions The person skilled in the art is aware that, if not stated explicitly, the expressions "a" or "an" as used in the present application may, depending on the situation, mean "one (1)", "one (1) or more" or "at least one (1)". For all the structures described herein, such as ring systems and groups, adjacent atoms must not be -O- O- or -O-S-. Structures having a variable number of possible carbon atoms (C atoms) may be referred to in the present application as Clower limit of carbon atoms-Cupper limit of carbon atoms structures (CLL-CUL structures), in order thus to be stipulated more specifically. Example: an alkyl group may consist of 3 to 10 carbon atoms and in that case corresponds to C3-C10alkyl. Ring structures composed of carbon atoms and heteroatoms may be referred to as "LL- to UL-membered" structures. One example of a 6-membered ring structure is toluene (a 6- membered ring structure substituted by a methyl group). If a collective term for a substituent, for example CLL-CULalkyl, is at the end of a composite substituent, for example CLL-CULcycloalkyl-CLL-CULalkyl, the constituent at the start of the composite substituent, for example the CLL-CULcycloalkyl, may be mono- or polysubstituted identically or differently and independently by the latter substituent, for example CLL-CULalkyl. All the collective terms used in this application for chemical groups, cyclic systems and cyclic groups can be stipulated more specifically through the addition "CLL-CUL" or "LL- to UL-membered". In the definitions of the symbols given in the above formulae, collective terms which are generally representative of the following substituents were used: Halogen relates to elements of the 7th main group, preferably fluorine, chlorine, bromine and iodine, more preferably fluorine, chlorine and bromine, and even more preferably fluorine and chlorine. Examples of heteroatom are N, O, S, P, B, Si. Preferably, the term "heteroatom" relates to N, S and O. According to the invention, "alkyl" – on its own or as part of a chemical group – represents straight-chain or branched hydrocarbons preferably having 1 to 6 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,2- dimethylpropyl, 1,1-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl, 2- methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,2-dimethylpropyl, 1,3-dimethylbutyl, 1,4- dimethylbutyl, 2,3-dimethylbutyl, 1,1-dimethylbutyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, 1,1,2- trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethylbutyl and 2-ethylbutyl. Preference is also given to alkyls having 1 to 4 carbon atoms such as, inter alia, methyl, ethyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl or t-butyl. The inventive alkyls may be substituted by one or more identical or different radicals. According to the invention, "alkenyl" – on its own or as part of a chemical group – represents straight- chain or branched hydrocarbons preferably having 2 to 6 carbon atoms and at least one double bond, for example vinyl, 2-propenyl, 2-butenyl, 3-butenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3- butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-2-propenyl, 1- ethyl-2-propenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2- pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1- methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2- butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-2- butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 1-ethyl-2-butenyl, 1- ethyl-3-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2- propenyl and 1-ethyl-2-methyl-2-propenyl. Preference is also given to alkenyls having 2 to 4 carbon atoms such as, inter alia, 2-propenyl, 2-butenyl or 1-methyl-2-propenyl. The inventive alkenyls may be substituted by one or more identical or different radicals. According to the invention, "alkynyl" – on its own or as part of a chemical group – represents straight- chain or branched hydrocarbons preferably having 2 to 6 carbon atoms and at least one triple bond, for example 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1- methyl-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2- propynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1- methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2- pentynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-3-butynyl, 2- ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl and 2,5-hexadiynyl. Preference is also given to alkynyls having 2 to 4 carbon atoms such as, inter alia, ethynyl, 2-propynyl or 2-butynyl-2-propenyl. The inventive alkynyls may be substituted by one or more identical or different radicals. According to the invention, "cycloalkyl" – on its own or as part of a chemical group – represents mono-, bi- or tricyclic hydrocarbons preferably having 3 to 10 carbons, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, bicyclo[2.2.1]heptyl, bicyclo[2.2.2]octyl or adamantyl. Preference is also given to cycloalkyls having 3, 4, 5, 6 or 7 carbon atoms such as, inter alia, cyclopropyl or cyclobutyl. The inventive cycloalkyls may be substituted by one or more identical or different radicals. According to the invention, "alkylcycloalkyl" represents mono-, bi- or tricyclic alkylcycloalkyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example methylcyclopropyl, ethylcyclopropyl, isopropylcyclobutyl, 3-methylcyclopentyl and 4-methylcyclohexyl. Preference is also given to alkylcycloalkyls having 4, 5 or 7 carbon atoms such as, inter alia, ethylcyclopropyl or 4-methylcyclohexyl. The inventive alkylcycloalkyls may be substituted by one or more identical or different radicals. According to the invention, "cycloalkylalkyl" represents mono-, bi- or tricyclic cycloalkylalkyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl and cyclopentylethyl. Preference is also given to cycloalkylalkyls having 4, 5 or 7 carbon atoms such as, inter alia, cyclopropylmethyl or cyclobutylmethyl. The inventive cycloalkylalkyls may be substituted by one or more identical or different radicals. According to the invention, "hydroxyalkyl" represents a straight-chain or branched alcohol preferably having 1 to 6 carbon atoms, for example methanol, ethanol, n-propanol, isopropanol (isopropan-2-ol), n- butanol, isobutanol, s-butanol and t-butanol. Preference is also given to hydroxyalkyl groups having 1 to 4 carbon atoms. The inventive hydroxyalkyl groups may be substituted by one or more identical or different radicals. According to the invention, "alkoxy" represents a straight-chain or branched O-alkyl preferably having 1 to 6 carbon atoms, for example methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, s-butoxy and t-butoxy. Preference is also given to alkoxy groups having 1 to 4 carbon atoms. The inventive alkoxy groups may be substituted by one or more identical or different radicals. According to the invention, "cycloalkoxy" represents a -O-cycloalkyl group, wherein cycloalkyl has the meaning as defined supra. Preference is given to cycloalkyls having 3, 4, 5, 6 or 7 carbon atoms, i.e. inter alia, -O-cyclopropyl,- O-cyclobutyl, -O-cyclopentyl, -O-cyclohexyl, -O-cycloheptyl. The inventive cycloalkoxy groups may be substituted by one or more identical or different radicals, preferably optional substituents are selected from halogens. According to the invention, "alkylthio", or “alkylsulfanyl”, represents straight-chain or branched S-alkyl preferably having 1 to 6 carbon atoms, for example methylthio, ethylthio, n-propylthio, isopropylthio, n- butylthio, isobutylthio, s-butylthio and t-butylthio. Preference is also given to alkylthio groups having 1 to 4 carbon atoms. The inventive alkylthio groups may be substituted by one or more identical or different radicals. According to the invention, "alkylsulfinyl" represents straight-chain or branched alkylsulfinyl preferably having 1 to 6 carbon atoms, for example methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, s-butylsulfinyl and t-butylsulfinyl. Preference is also given to alkylsulfinyl groups having 1 to 4 carbon atoms. The inventive alkylsulfinyl groups may be substituted by one or more identical or different radicals. According to the invention, "alkylsulfonyl" represents straight-chain or branched alkylsulfonyl preferably having 1 to 6 carbon atoms, for example methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, s-butylsulfonyl and t-butylsulfonyl. Preference is also given to alkylsulfonyl groups having 1 to 4 carbon atoms. The inventive alkylsulfonyl groups may be substituted by one or more identical or different radicals. According to the invention, “cycloalkylsulfonyl” represents mono-, bi- or tricyclic cycloalkylsulfonyl preferably having 4 to 10 or 4 to 7 carbon atoms, for example cyclopropylsulfonyl, cyclobutylsulfonyl, cyclopentylsulfonyl and cyclohexylsulfonyl. Preference is also given to cycloalkylsulfonyls having 4, 5 or 7 carbon atoms such as, inter alia, cyclopropylsulfonyl or cyclobutylsulfonal. The inventive cycloalkylsulfonyls may be substituted by one or more identical or different radicals. If used herein, the term "alkylcarbonyl" represents straight-chain or branched alkyl-C(=O) preferably having 2 to 7 carbon atoms such as methylcarbonyl, ethylcarbonyl, n-propylcarbonyl, isopropylcarbonyl, s-butylcarbonyl and t-butylcarbonyl. Preference is also given to alkylcarbonyls having 1 to 4 carbon atoms. Alkylcarbonyls may be substituted by one or more identical or different radicals. If used herein, the term "alkoxycarbonyl" - alone or as a constituent of a chemical group - represents straight-chain or branched alkoxycarbonyl, preferably having 1 to 6 carbon atoms or having 1 to 4 carbon atoms in the alkoxy moiety, for example methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, isopropoxycarbonyl, s-butoxycarbonyl and t-butoxycarbonyl. Alkoxycarbonyl groups may be substituted by one or more identical or different radicals. If used herein, the term "alkylaminocarbonyl" represents straight-chain or branched alkylaminocarbonyl having preferably 1 to 6 carbon atoms or 1 to 4 carbon atoms in the alkyl moiety, for example methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl, s- butylaminocarbonyl and t-butylaminocarbonyl. Alkylaminocarbonyl groups may be substituted by one or more identical or different radicals. If used herein, the term "N,N-dialkylaminocarbonyl" represents straight-chain or branched N,N- dialkylaminocarbonyl having preferably 1 to 6 carbon atoms or 1 to 4 carbon atoms in the alkyl moiety, for example N,N-dimethylaminocarbonyl, N,N-diethylaminocarbonyl, N,N-di(n-propylamino)carbonyl, N,N-di(isopropylamino)carbonyl and N,N-di-(s-butylamino)carbonyl. N,N-dialkylaminocarbonyl groups may be substituted by one or more identical or different radicals. Generally, the term "aryl" represents a mono-, bi- or polycyclic aromatic system having preferably 6 to 14, especially 6 to 10, ring carbon atoms, for example phenyl, naphthyl, anthryl, phenanthrenyl, preferably phenyl. Aryl may also represent polycyclic systems, including fused polycyclic systems, such as tetrahydronaphthyl, indenyl, indanyl, fluorenyl, biphenyl, where the bonding site is on the aromatic system. A fused polycyclic system has at least two fused rings, wherein these two fused rings share two adjacent atoms (or, iIn other words, the rings share one covalent bond). Preference is given to phenyl. The inventive aryl groups, in particular phenyl groups, may be substituted by one or more identical or different radicals. According to the invention the term “polycyclic” ring refers to fused, bridged and spirocyclic carbocyclic and heterocyclic rings as well as ring systems linked through single or double bonds. According to the invention, "heterocycle", "heterocyclic ring" or "heterocyclic ring system" represents a carbocyclic ring system having at least one ring in which at least one carbon atom is replaced by a heteroatom, preferably by a heteroatom from the group consisting of N, O, S, P, B, Si, Se, and which is saturated, unsaturated or heteroaromatic and may be unsubstituted or substituted, where the bonding site is on a ring atom. Unless defined differently, the heterocyclic ring contains 3 to 12 ring atoms, preferably 3 to 9 ring atoms, especially 3 to 6 ring atoms, and one or more, preferably 1 to 4, especially 1, 2 or 3, heteroatoms in the heterocyclic ring, preferably from the group consisting of N, O, and S, although no two oxygen atoms should be directly adjacent. The heterocyclic rings usually contain not more than 4 nitrogen atoms and/or not more than 2 oxygen atoms and/or not more than 2 sulphur atoms. Non-aromatic heterocycles herein are usually referred to as “saturated or unsatured heterocycle”. When the heterocyclyl radical or the heterocyclic ring is optionally substituted, it may be fused to other carbocyclic or heterocyclic rings. In the case of optionally substituted heterocyclyl, the invention also embraces polycyclic systems, for example 8-azabicyclo[3.2.1]octanyl, 1-azabicyclo[2.2.1]heptyl, 1-oxa-5- azaspiro[2.3]hexyl or 2,3-dihydro-1H-indole. In the case of optionally substituted heterocyclyl, the invention also embraces spirocyclic systems, for example 1-oxa-5-azaspiro[2.3]hexyl. Preferred heterocyclyl groups of the invention are, for example, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, dihydropyranyl, tetrahydropyranyl, dioxanyl, pyrrolinyl, pyrrolidinyl, imidazolinyl, imidazolidinyl, thiazolidinyl, oxazolidinyl, dioxolanyl, dioxolyl, pyrazolidinyl, tetrahydrofuranyl, dihydrofuranyl, oxetanyl, oxiranyl, azetidinyl, aziridinyl, oxazetidinyl, oxaziridinyl, oxazepanyl, oxazinanyl, azepanyl, oxopyrrolidinyl, dioxopyrrolidinyl, oxomorpholinyl, oxopiperazinyl and oxepanyl. Most preferred is oxetanyl, tetrahydropyranyl and piperazinyl. Of particular significance are heteroaryls, i.e. heteroaromatic systems. According to the invention, the term heteroaryl represents heteroaromatic compounds, i.e. completely unsaturated aromatic heterocyclic compounds which fall under the above definition of heterocycles. For clarification, if the definition of a substituent herein includes “heterocycle” (or “heterocyclyl”) as well as “heteroaryl” (or “heteroaromatic”) this means that the term “heterocycle” (or “heterocyclyl”) does not include “heteroaryl” (or “heteroaromatic”) groups in order to avoid an overlap of definitions. Preference is given to 5- to 7- membered rings, more preferably 6- or 6-membered rings, having 1 to 3, preferably 1 or 2, identical or different heteroatoms from the groups above. Inventive heteroaryls are, for example, furyl, thienyl, pyrazolyl, imidazolyl, 1,2,3- and 1,2,4-triazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-, 1,3,4-, 1,2,4- and 1,2,5-oxadiazolyl, azepinyl, pyrrolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1,3,5-, 1,2,4- and 1,2,3-triazinyl, 1,2,4-, 1,3,2-, 1,3,6- and 1,2,6-oxazinyl, oxepinyl, thiepinyl, 1,2,4-triazolonyl and 1,2,4- diazepinyl. Preference is given to pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrazolyl, pyrrolyl, thiazolyl, oxazolyl, isothiazolyl, and isoxazolyl. More preferred are pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, pyrazolyl, pyrrolyl, and thiazolyl. The inventive heteroaryl groups may also be substituted by one or more identical or different radicals. The term “in each case optionally substituted” means that a group/substituent , such as a alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, cycloalkyl, aryl, phenyl, benzyl, heterocyclyl and heteroaryl radical etc., may be substituted, meaning, for example, a substituted radical derived from the unsubstituted base structure, where the substituents, for example, one (1) substituent or a plurality of substituents, preferably 1, 2, 3, 4, 5, 6 or 7, more preferably 1, 2, 3 or 4 substituents, more preferably 1, 2 or 3 substituents, even more preferred 1 or 2 substituents, are independently selected from a group consisting of amino, hydroxyl, halogen, nitro, cyano, isocyano, mercapto, isothiocyanato, C1-C4carboxyl, carbonamide, SF5, aminosulphonyl, C1-C4alkyl, C1-C4haloalkyl C3-C4cycloalkyl, C2-C4alkenyl, C5- C6cycloalkenyl, C2-C4alkynyl, N-mono-C1-C4alkylamino, N,N-di-C1-C4alkylamino, N-C1- C4alkanoylamino, C1-C4alkoxy, C1-C4haloalkoxy, C2-C4alkenyloxy, C2-C4alkynyloxy, C3-C4cycloalkoxy, C5-C6cycloalkenyloxy, C1-C4alkoxycarbonyl, C2-C4alkenyloxycarbonyl, C2-C4alkynyloxycarbonyl, C6- ,C10-,C14-aryloxycarbonyl, C1-C4alkanoyl, C2-C4alkenylcarbonyl, C2-C4alkynylcarbonyl, C6-,C10-,C14- arylcarbonyl, C1-C4alkylthio, C1-C4haloalkylthio, C3-C4cycloalkylthio, C2-C4alkenylthio, C5- C6cycloalkenylthio, C2-C4alkynylthio, C1-C4alkylsulfinyl, including both enantiomers of the C1- C4alkylsulfinyl group, C1-C4haloalkylsulfinyl, including both enantiomers of the C1-C4haloalkylsulfinyl group, C1-C4alkylsulfonyl, C1-C4haloalkylsulfonyl, N-mono-C1-C4alkylaminosulfonyl, N,N-di-C1- C4alkylaminosulfonyl, C1-C4alkylphosphinyl, C1-C4alkylphosphonyl, including both enantiomers of C1- C4alkylphosphinyl and C1-C4alkylphosphonyl, N-C1-C4alkylaminocarbonyl, N,N-di-C1- C4alkylaminocarbonyl, N-C1-C4alkanoylaminocarbonyl, N-C1-C4alkanoyl-N-C1-C4alkylaminocarbonyl, C6-,C10-,C14-aryl, C6-,C10-,C14-aryloxy, benzyl, benzyloxy, benzylthio, C6-,C10-,C14-arylthio, C6-,C10-,C14- arylamino, benzylamino, heterocyclyl and trialkylsilyl ((C1-C4alkyl)3-silyl), substituents bonded via a double bond, such as C1-C4alkylidene (e.g. methylidene or ethylidene), an oxo group, an imino group and a substituted imino group. When two or more radicals form one or more rings, these may be carbocyclic, heterocyclic, saturated, partly saturated, unsaturated, for example including aromatic rings and with further substitution. The substituents mentioned by way of example ("first substituent level") may, if they contain hydrocarbonaceous components, optionally have further substitution therein ("second substituent level"), for example by one or more of the substituents each independently selected from halogen, hydroxyl, C1-C6alkyl, amino, nitro, cyano, isocyano, azido, acylamino, an oxo group and an imino group. The term "(optionally) substituted" group preferably embraces just one or two substituent levels. The inventive halogen-substituted chemical groups or halogenated groups (for example alkyl, cycloalkyl, alkoxy, alkylthio, alkylsulfinyl, or alkylsulfonyl etc.) are mono- or polysubstituted by halogen up to the maximum possible number of substituents. Such groups are also referred to as halo groups (for example haloalkyl, halocycloalkyl, haloalkoxy, haloalkylthio, haloalkylsulfinyl, or haloalkylsulfonyl etc.). In the case of polysubstitution by halogen, the halogen atoms may be the same or different, and may all be bonded to one carbon atom or may be bonded to a plurality of carbon atoms. Halogen is especially fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine and more preferably fluorine or chlorine, even more preferred is fluorine. More particularly, halogen-substituted groups are monohalocycloalkyl such as 1-fluorocyclopropyl, 2-fluorocyclopropyl or 1-fluorocyclobutyl, monohaloalkyl such as 2-chloroethyl, 2-fluoroethyl, 1-chloroethyl, 1-fluoroethyl, chloromethyl, or fluoromethyl; perhaloalkyl such as trichloromethyl or trifluoromethyl or CF2CF3, polyhaloalkyl such as difluoromethyl, 2-fluoro-2-chloroethyl, dichloromethyl, 1,1,2,2-tetrafluoroethyl or 2,2,2-trifluoroethyl. Further examples of haloalkyls are trichloromethyl, chlorodifluoromethyl, dichlorofluoromethyl, chloromethyl, bromomethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2,2,2- trichloroethyl, 2-chloro-2,2-difluoroethyl, pentafluoroethyl, 3,3,3-trifluoropropyl and pentafluoro-t-butyl. Preference is given to haloalkyls having 1 to 4 carbon atoms and 1 to 9, preferably 1 to 5, identical or different halogen atoms selected from fluorine, chlorine and bromine. Particular preference is given to haloalkyls having 1 or 2 carbon atoms and 1 to 5 identical or different halogen atoms selected from fluorine and chlorine, such as, inter alia, difluoromethyl, trifluoromethyl or 2,2-difluoroethyl. Further examples of halogen-substituted compounds are haloalkoxy such as OCF3, OCHF2, OCH2F, OCF2CF3, OCH2CF3, OCH2CHF2 und OCH2CH2Cl; haloalkylsulfanyls such as difluoromethylthio, trifluoromethylthio, trichloromethylthio, chlorodifluoromethylthio, 1-fluoroethylthio, 2-fluoroethylthio, 2,2-difluoroethylthio, 1,1,2,2-tetrafluoroethylthio, 2,2,2-trifluoroethylthio or 2-chloro-1,1,2-trifluoroethylthio; haloalkylsulfinyls such as difluoromethylsulfinyl, trifluoromethylsulfinyl, trichloromethylsulfinyl, chlorodifluoromethylsulfinyl, 1-fluoroethylsulfinyl, 2-fluoroethylsulfinyl, 2,2-difluoroethylsulfinyl, 1,1,2,2-tetrafluoroethylsulfinyl, 2,2,2-trifluoroethylsulfinyl and 2-chloro-1,1,2-trifluoroethylsulfinyl; haloalkylsulfonyl groups such as difluoromethylsulfonyl, trifluoromethylsulfonyl, trichloromethylsulfonyl, chlorodifluoromethylsulfonyl, 1-fluoroethylsulfonyl, 2-fluoroethylsulfonyl, 2,2- difluoroethylsulfonyl, 1,1,2,2-tetrafluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl and 2-chloro-1,1,2- trifluoroethylsulfonyl. The inventive cyano-substituted chemical groups (for example alkyl, cycloalkyl, alkoxy, alkylthio, alkylsulfinyl, or alkylsulfonyl etc.) are preferably monosubstituted by cyano. Such cyano-substituted groups are also referred to as cyano groups (for example cyanoalkyl, cyanocycloalkyl, cyanoalkoxy, cyanoalkylthio, cyanoalkylsulfinyl, cyanoalkylsufonyl etc.). If the number of carbon atoms is specified in such cyano groups, for example CLL-ULcyanoalkyl, the carbon atom of the cyano group will not be counted; e.g. C1-3cyanoalkyl includes cyanopropyl groups. In the case of radicals having carbon atoms, preference is given to those having 1 to 4 carbon atoms, especially 1 or 2 carbon atoms. Preference is generally given to substituents from the group of halogen, e.g. fluorine and chlorine, (C1-C4)alkyl, preferably methyl or ethyl, (C1-C4)haloalkyl, preferably trifluoromethyl, (C1-C4)alkoxy, preferably methoxy or ethoxy, (C1-C4)haloalkoxy, nitro and cyano. Particular preference is given here to the substituents methyl, methoxy, fluorine, chlorine, bromine and cyano. Substituted amino such as mono- or disubstituted amino means a radical from the group of the substituted amino radicals which are N-substituted, for example, by one or two identical or different radicals from the group of alkyl, hydroxy, amino, alkoxy, acyl and aryl; preferably N-mono- and N,N-dialkylamino, (for example methylamino, ethylamino, N,N-dimethylamino, N,N-diethylamino, N,N-di-n-propylamino, N,N- diisopropylamino or N,N-dibutylamino), N-mono- or N,N-dialkoxyalkylamino groups (for example N- methoxymethylamino, N-methoxyethylamino, N,N-di(methoxymethyl)amino or N,N- di(methoxyethyl)amino), N-mono- and N,N-diarylamino, such as optionally substituted anilines, acylamino, N,N-diacylamino, N-alkyl-N-arylamino, N-alkyl-N-acylamino and also saturated N- heterocycles; preference is given here to alkyl radicals having 1 to 4 carbon atoms; here, aryl is preferably phenyl or substituted phenyl; for acyl, the definition given further below applies, preferably (C1-C4)- alkanoyl. The same applies to substituted hydroxylamino or hydrazino. Substituted amino also includes quaternary ammonium compounds (salts) having four organic substituents on the nitrogen atom. Optionally substituted phenyl is preferably phenyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals from the group of halogen, SF5, (C1- C4)alkyl, C3-C6cycloalkyl, (C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkyl, (C1-C4)haloalkyl, (C1-C4)haloalkoxy, hydroxy-C1-C4alkyl, (C1-C4)alkylthio, (C1-C4)haloalkylthio, (C1- C4)alkylsulfinyl (C1-C4) haloalkylsulfinyl, (C1-C4)alkylsulfonyl (C1-C4)haloalkylsulfonyl, cyano, isocyano and nitro, for example o-, m- and p-tolyl, dimethylphenyls, 2-, 3- and 4-chlorophenyl, 2-, 3- and 4-fluorophenyl, 2-, 3- and 4-trifluoromethyl- and 4-trichloromethylphenyl, 2,4-, 3,5-, 2,5- and 2,3- dichlorophenyl, o-, m- and p-methoxyphenyl, 4-heptafluorophenyl. Optionally substituted cycloalkyl is preferably cycloalkyl which is unsubstituted or mono- or polysubstituted, preferably up to trisubstituted, by identical or different radicals from the group of halogen, cyano, (C1-C4)alkyl, (C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkoxy, (C1-C4)alkoxy-(C1-C4)alkyl, (C1- C4)haloalkyl and (C1-C4)haloalkoxy, especially by one or two (C1-C4)alkyl radicals. Inventive compounds may occur in preferred embodiments. Individual embodiments described herein may be combined with one another. Not included are combinations which contravene the laws of nature and which the person skilled in the art would therefore rule out on the basis of his/her expert knowledge. Ring structures having three or more adjacent oxygen atoms, for example, are excluded. Isomers Depending on the nature of the substituents, the compounds of the formula (I) may be in the form of geometric and/or optically active isomers or corresponding isomer mixtures in different compositions. These stereoisomers are, for example, enantiomers, diastereomers, atropisomers or geometric isomers. Accordingly, the invention encompasses both pure stereoisomers and any mixture of these isomers. Methods and uses The invention also relates to methods for controlling animal pests, in which compounds of the formula (I) are allowed to act on animal pests and/or their habitat. The control of the animal pests is preferably conducted in agriculture and forestry, and in material protection. Preferably excluded herefrom are methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods carried out on the human or animal body. The invention furthermore relates to the use of the compounds of the formula (I) as pesticides, in particular crop protection agents. In the context of the present application, the term "pesticide" in each case also always comprises the term "crop protection agent". The compounds of the formula (I), having good plant tolerance, favourable homeotherm toxicity and good environmental compatibility, are suitable for protecting plants and plant organs against biotic and abiotic stressors, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, especially insects, arachnids, helminths, in particular nematodes, and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in aquatic cultures, in forests, in gardens and leisure facilities, in the protection of stored products and of materials, and in the hygiene sector. Within the context of the present patent application, the term “hygiene” is understood to mean any and all measures, procedures and practices which aim to prevent disease, in particular infectious disease, and which serve to protect the health of humans and animals and/or to protect the environment, and/or which maintain cleanliness. In accordance with the invention, this especially includes measures for cleaning, disinfection and sterilisation of, for example, textiles or hard surfaces, especially surfaces of glass, wood, concrete, porcelain, ceramics, plastic or also of metal(s), and for ensuring that these are kept free of hygiene pests and/or their excretions. Preferably excluded from the scope of the invention in this regard are surgical or therapeutic treatment procedures applicable to the human body or to the bodies of animals and diagnostic procedures which are carried out on the human body or on the bodies of animals. The term “hygiene sector” thus covers all areas, technical fields and industrial applications in which these hygiene measures, procedures and practices are important, in relation for example to hygiene in kitchens, bakeries, airports, bathrooms, swimming pools, department stores, hotels, hospitals, stables, animal husbandries, etc. The term “hygiene pest” is therefore understood to mean one or more animal pests whose presence in the hygiene sector is problematic, in particular for health reasons. It is therefore a primary objective to avoid or minimize the presence of hygiene pests, and/or exposure to them, in the hygiene sector. This can be achieved in particular through the application of a pesticide that can be used both to prevent infestation and to tackle an infestation which is already present. Preparations which avoid or reduce exposure to pests can also be used. Hygiene pests include, for example, the organisms mentioned below. The term “hygiene protection” thus covers all actions to maintain and/or improve these hygiene measures, procedures and practices. The compounds of the formula (I) can preferably be used as pesticides. They are active against normally sensitive and resistant species and against all or some stages of development. The abovementioned pests include: pests from the phylum of the Arthropoda, in particular from the class of the Arachnida, for example Acarus spp., for example Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., for example Aculus fockeui, Aculus schlechtendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., for example Brevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., for example Eotetranychus hicoriae, Epitrimerus pyri, Eutetranychus spp., for example Eutetranychus banksi, Eriophyes spp., for example Eriophyes pyri, Glycyphagus domesticus, Halotydeus destructor, Hemitarsonemus spp., for example Hemitarsonemus latus (=Polyphagotarsonemus latus), Hyalomma spp., Ixodes spp., Latrodectus spp., Loxosceles spp., Neutrombicula autumnalis, Nuphersa spp., Oligonychus spp., for example Oligonychus coffeae, Oligonychus coniferarum, Oligonychus ilicis, Oligonychus indicus, Oligonychus mangiferus, Oligonychus pratensis, Oligonychus punicae, Oligonychus yothersi, Ornithodorus spp., Ornithonyssus spp., Panonychus spp., for example Panonychus citri (=Metatetranychus citri), Panonychus ulmi (=Metatetranychus ulmi), Phyllocoptruta oleivora, Platytetranychus multidigituli, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Steneotarsonemus spp., Steneotarsonemus spinki, Tarsonemus spp., for example Tarsonemus confusus, Tarsonemus pallidus, Tetranychus spp., for example Tetranychus canadensis, Tetranychus cinnabarinus, Tetranychus turkestani, Tetranychus urticae, Trombicula alfreddugesi, Vaejovis spp., Vasates lycopersici; from the class of the Chilopoda, for example Geophilus spp., Scutigera spp.; from the order or the class of the Collembola, for example Onychiurus armatus; Sminthurus viridis; from the class of the Diplopoda, for example Blaniulus guttulatus; from the class of the Insecta, for example from the order of the Blattodea, for example Blatta orientalis, Blattella asahinai, Blattella germanica, Leucophaea maderae, Loboptera decipiens, Neostylopyga rhombifolia, Panchlora spp., Parcoblatta spp., Periplaneta spp., for example Periplaneta americana, Periplaneta australasiae, Pycnoscelus surinamensis, Supella longipalpa; from the order of the Coleoptera, for example Acalymma vittatum, Acanthoscelides obtectus, Adoretus spp., Aethina tumida, Agelastica alni, Agrilus spp., for example Agrilus planipennis, Agrilus coxalis, Agrilus bilineatus, Agrilus anxius, Agriotes spp., for example Agriotes linneatus, Agriotes mancus, Alphitobius diaperinus, Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., for example Anoplophora glabripennis, Anthonomus spp., for example Anthonomus grandis, Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., for example Atomaria linearis, Attagenus spp., Baris caerulescens, Bruchidius obtectus, Bruchus spp., for example Bruchus pisorum, Bruchus rufimanus, Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., for example Ceutorrhynchus assimilis, Ceutorrhynchus quadridens, Ceutorrhynchus rapae, Chaetocnema spp., for example Chaetocnema confinis, Chaetocnema denticulata, Chaetocnema ectypa, Cleonus mendicus, Conoderus spp., Cosmopolites spp., for example Cosmopolites sordidus, Costelytra zealandica, Ctenicera spp., Curculio spp., for example Curculio caryae, Curculio caryatrypes,Curculio obtusus, Curculio sayi, Cryptolestes ferrugineus, Cryptolestes pusillus, Cryptorhynchus lapathi, Cryptorhynchus mangiferae, Cylindrocopturus spp., Cylindrocopturus adspersus, Cylindrocopturus furnissi, Dendroctonus spp., for example Dendroctonus ponderosae, Dermestes spp., Diabrotica spp., for example Diabrotica balteata, Diabrotica barberi, Diabrotica undecimpunctata howardi, Diabrotica undecimpunctata undecimpunctata, Diabrotica virgifera virgifera, Diabrotica virgifera zeae, Dichocrocis spp., Dicladispa armigera, Diloboderus spp., Epicaerus spp., Epilachna spp., for example Epilachna borealis, Epilachna varivestis, Epitrix spp., for example Epitrix cucumeris, Epitrix fuscula, Epitrix hirtipennis, Epitrix subcrinita, Epitrix tuberis, Faustinus spp., Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypomeces squamosus, Hypothenemus spp., for example Hypothenemus hampei, Hypothenemus obscurus, Hypothenemus pubescens, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp., Leptinotarsa decemlineata, Leucoptera spp., for example Leucoptera coffeella, Limonius ectypus, Lissorhoptrus oryzophilus, Listronotus (= Hyperodes) spp., Lixus spp., Luperodes spp., Luperomorpha xanthodera, Lyctus spp., Megacyllene spp., for example Megacyllene robiniae, Megascelis spp., Melanotus spp., for example Melanotus longulus oregonensis, Meligethes aeneus, Melolontha spp., for example Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Necrobia spp., Neogalerucella spp., Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorhynchus spp., for example Otiorhynchus cribricollis, Otiorhynchus ligustici, Otiorhynchus ovatus, Otiorhynchus rugosostriarus, Otiorhynchus sulcatus, Oulema spp., for example Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Phyllophaga helleri, Phyllotreta spp., for example Phyllotreta armoraciae, Phyllotreta pusilla, Phyllotreta ramosa, Phyllotreta striolata, Popillia japonica, Premnotrypes spp., Prostephanus truncatus, Psylliodes spp., for example Psylliodes affinis, Psylliodes chrysocephala, Psylliodes punctulata, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Rhynchophorus spp., Rhynchophorus ferrugineus, Rhynchophorus palmarum, Scolytus spp., for example Scolytus multistriatus, Sinoxylon perforans, Sitophilus spp., for example Sitophilus granarius, Sitophilus linearis, Sitophilus oryzae, Sitophilus zeamais, Sphenophorus spp., Stegobium paniceum, Sternechus spp., for example Sternechus paludatus, Symphyletes spp., Tanymecus spp., for example Tanymecus dilaticollis, Tanymecus indicus, Tanymecus palliatus, Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., for example Tribolium audax, Tribolium castaneum, Tribolium confusum, Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp., for example Zabrus tenebrioides; from the order of the Dermaptera, for example Anisolabis maritime, Forficula auricularia, Labidura riparia; from the order of the Diptera, for example Aedes spp., for example Aedes aegypti, Aedes albopictus, Aedes sticticus, Aedes vexans, Agromyza spp., for example Agromyza frontella, Agromyza parvicornis, Anastrepha spp., Anopheles spp., for example Anopheles quadrimaculatus, Anopheles gambiae, Asphondylia spp., Bactrocera spp., for example Bactrocera cucurbitae, Bactrocera dorsalis, Bactrocera oleae, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chironomus spp., Chrysomya spp., Chrysops spp., Chrysozona pluvialis, Cochliomya spp., Contarinia spp., for example Contarinia johnsoni, Contarinia nasturtii, Contarinia pyrivora, Contarinia schulzi, Contarinia sorghicola, Contarinia tritici,Cordylobia anthropophaga, Cricotopus sylvestris, Culex spp., for example Culex pipiens, Culex quinquefasciatus, Culicoides spp., Culiseta spp., Cuterebra spp., Dacus oleae, Dasineura spp., for example Dasineura brassicae, Delia spp., for example Delia antiqua, Delia coarctata, Delia florilega, Delia platura, Delia radicum, Dermatobia hominis, Drosophila spp., for example Drosphila melanogaster, Drosophila suzukii, Echinocnemus spp., Euleia heraclei, Fannia spp., Gasterophilus spp., Glossina spp., Haematopota spp., Hydrellia spp., Hydrellia griseola, Hylemya spp., Hippobosca spp., Hypoderma spp., Liriomyza spp., for example Liriomyza brassicae, Liriomyza huidobrensis, Liriomyza sativae, Lucilia spp., for example Lucilia cuprina, Lutzomyia spp., Mansonia spp., Musca spp., for example Musca domestica, Musca domestica vicina, Oestrus spp., Oscinella frit, Paratanytarsus spp., Paralauterborniella subcincta, Pegomya or Pegomyia spp., for example Pegomya betae, Pegomya hyoscyami, Pegomya rubivora, Phlebotomus spp., Phorbia spp., Phormia spp., Piophila casei, Platyparea poeciloptera, Prodiplosis spp., Psila rosae, Rhagoletis spp., for example Rhagoletis cingulata, Rhagoletis completa, Rhagoletis fausta, Rhagoletis indifferens, Rhagoletis mendax, Rhagoletis pomonella, Sarcophaga spp., Simulium spp., for example Simulium meridionale, Stomoxys spp., Tabanus spp., Tetanops spp., Tipula spp., for example Tipula paludosa, Tipula simplex, Toxotrypana curvicauda; from the order of the Hemiptera, for example Acizzia acaciaebaileyanae, Acizzia dodonaeae, Acizzia uncatoides, Acrida turrita, Acyrthosipon spp., for example Acyrthosiphon pisum, Acrogonia spp., Aeneolamia spp., Agonoscena spp., Aleurocanthus spp., Aleyrodes proletella, Aleurolobus barodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrasca spp., for example Amrasca bigutulla, Amrasca devastans, Anuraphis cardui, Aonidiella spp., for example Aonidiella aurantii, Aonidiella citrina, Aonidiella inornata, Aphanostigma piri, Aphis spp., for example Aphis citricola, Aphis craccivora, Aphis fabae, Aphis forbesi, Aphis glycines, Aphis gossypii, Aphis hederae, Aphis illinoisensis, Aphis middletoni, Aphis nasturtii, Aphis nerii, Aphis pomi, Aphis spiraecola, Aphis viburniphila, Arboridia apicalis, Arytainilla spp., Aspidiella spp., Aspidiotus spp., for example Aspidiotus nerii, Atanus spp., Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp., for example Cacopsylla pyricola, Calligypona marginata, Capulinia spp., Carneocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chondracris rosea, Chromaphis juglandicola, Chrysomphalus aonidum, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halli, Coccus spp., for example Coccus hesperidum, Coccus longulus, Coccus pseudomagnoliarum, Coccus viridis, Cryptomyzus ribis, Cryptoneossa spp., Ctenarytaina spp., Dalbulus spp., Dialeurodes chittendeni, Dialeurodes citri, Diaphorina citri, Diaspis spp., Diuraphis spp., Doralis spp., Drosicha spp., Dysaphis spp., for example Dysaphis apiifolia, Dysaphis plantaginea, Dysaphis tulipae, Dysmicoccus spp., Empoasca spp., for example Empoasca abrupta, Empoasca fabae, Empoasca maligna, Empoasca solana, Empoasca stevensi, Eriosoma spp., for example Eriosoma americanum, Eriosoma lanigerum, Eriosoma pyricola, Erythroneura spp., Eucalyptolyma spp., Euphyllura spp., Euscelis bilobatus, Ferrisia spp., Fiorinia spp., Furcaspis oceanica, Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus pruni, Icerya spp., for example Icerya purchasi, Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., for example Lecanium corni (=Parthenolecanium corni), Lepidosaphes spp., for example Lepidosaphes ulmi, Lipaphis erysimi, Lopholeucaspis japonica, Lycorma delicatula, Macrosiphum spp., for example Macrosiphum euphorbiae, Macrosiphum lilii, Macrosiphum rosae, Macrosteles facifrons, Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metcalfa pruinosa, Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., for example Myzus ascalonicus, Myzus cerasi, Myzus ligustri, Myzus ornatus, Myzus persicae,. Myzus nicotianae, Nasonovia ribisnigri, Neomaskellia spp., Nephotettix spp., for example Nephotettix cincticeps,, Nephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., for example Paratrioza cockerelli, Parlatoria spp., Pemphigus spp., for example Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccus spp., for example Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., for example Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., for example Planococcus citri, Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., for example Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseudococcus viburni, Psyllopsis spp., Psylla spp., for example Psylla buxi, Psylla mali, Psylla pyri, Pteromalus spp., Pulvinaria spp., Pyrilla spp., Quadraspidiotus spp., for example Quadraspidiotus juglansregiae, Quadraspidiotus ostreaeformis, Quadraspidiotus perniciosus, Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., for example Rhopalosiphum maidis, Rhopalosiphum oxyacanthae, Rhopalosiphum padi, Rhopalosiphum rufiabdominale, Saissetia spp., for example Saissetia coffeae, Saissetia miranda, Saissetia neglecta, Saissetia oleae, Scaphoideus titanus, Schizaphis graminum, Selenaspidus articulatus, Sipha flava, Sitobion avenae, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Siphoninus phillyreae, Tenalaphara malayensis,Tetragonocephela spp., Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., for example Toxoptera aurantii, Toxoptera citricidus, Trialeurodes vaporariorum, Trioza spp., for example Trioza diospyri, Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp.; from the suborder of the Heteroptera, for example Aelia spp., Anasa tristis, Antestiopsis spp., Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., for example Cimex adjunctus, Cimex hemipterus, Cimex lectularius, Cimex pilosellus, Collaria spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., for example Euschistus heros, Euschistus servus, Euschistus tristigmus, Euschistus variolarius, Eurydema spp., Eurygaster spp., Halyomorpha halys, Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptocorisa varicornis, Leptoglossus occidentalis, Leptoglossus phyllopus, Lygocoris spp., for example Lygocoris pabulinus, Lygus spp., for example Lygus elisus, Lygus hesperus, Lygus lineolaris, Macropes excavatus, Megacopta cribraria, Miridae, Monalonion atratum, Nezara spp., for example Nezara viridula, Nysius spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., for example Piezodorus guildinii, Psallus spp., Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.; from the order of the Hymenoptera, for example Acromyrmex spp., Athalia spp., for example Athalia rosae, Atta spp., Camponotus spp., Dolichovespula spp., Diprion spp., for example Diprion similis, Hoplocampa spp., for example Hoplocampa cookei, Hoplocampa testudinea, Lasius spp., Linepithema (Iridiomyrmex) humile, Monomorium pharaonis, Paratrechina spp., Paravespula spp., Plagiolepis spp., Sirex spp., for example Sirex noctilio, Solenopsis invicta, Tapinoma spp., Technomyrmex albipes, Urocerus spp., Vespa spp., for example Vespa crabro, Wasmannia auropunctata, Xeris spp.; from the order of the Isopoda, for example Armadillidium vulgare, Oniscus asellus, Porcellio scaber; from the order of the Isoptera, for example Coptotermes spp., for example Coptotermes formosanus, Cornitermes cumulans, Cryptotermes spp., Incisitermes spp., Kalotermes spp., Microtermes obesi, Nasutitermes spp., Odontotermes spp., Porotermes spp., Reticulitermes spp., for example Reticulitermes flavipes, Reticulitermes hesperus; from the order of the Lepidoptera, for example Achroia grisella, Acronicta major, Adoxophyes spp., for example Adoxophyes orana, Aedia leucomelas, Agrotis spp., for example Agrotis segetum, Agrotis ipsilon, Alabama spp., for example Alabama argillacea, Amyelois transitella, Anarsia spp., Anticarsia spp., for example Anticarsia gemmatalis, Argyroploce spp., Autographa spp., Barathra brassicae, Blastodacna atra, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp., Caloptilia theivora, Capua reticulana, Carpocapsa pomonella, Carposina niponensis, Cheimatobia brumata, Chilo spp., for example Chilo plejadellus, Chilo suppressalis, Choreutis pariana, Choristoneura spp., Chrysodeixis chalcites, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Cydia spp., for example Cydia nigricana, Cydia pomonella, Dalaca noctuides, Diaphania spp., Diparopsis spp., Diatraea saccharalis, Dioryctria spp., for example Dioryctria zimmermani, Earias spp., Ecdytolopha aurantium, Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., for example Ephestia elutella, Ephestia kuehniella, Epinotia spp., Epiphyas postvittana, Erannis spp., Erschoviella musculana, Etiella spp., Eudocima spp., Eulia spp., Eupoecilia ambiguella, Euproctis spp., for example Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Gracillaria spp., Grapholitha spp., for example Grapholita molesta, Grapholita prunivora, Hedylepta spp., Helicoverpa spp., for example Helicoverpa armigera, Helicoverpa zea, Heliothis spp., for example Heliothis virescens, Hofmannophila pseudospretella, Homoeosoma spp., Homona spp., Hyponomeuta padella, Kakivoria flavofasciata, Lampides spp., Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis, Leucoptera spp., for example Leucoptera coffeella, Lithocolletis spp., for example Lithocolletis blancardella, Lithophane antennata, Lobesia spp., for example Lobesia botrana, Loxagrotis albicosta, Lymantria spp., for example Lymantria dispar, Lyonetia spp., for example Lyonetia clerkella, Malacosoma neustria, Maruca testulalis, Mamestra brassicae, Melanitis leda, Mocis spp., Monopis obviella, Mythimna separata, Nemapogon cloacellus, Nymphula spp., Oiketicus spp., Omphisa spp., Operophtera spp., Oria spp., Orthaga spp., Ostrinia spp., for example Ostrinia nubilalis, Panolis flammea, Parnara spp., Pectinophora spp., for example Pectinophora gossypiella, Perileucoptera spp., Phthorimaea spp., for example Phthorimaea operculella, Phyllocnistis citrella, Phyllonorycter spp., for example Phyllonorycter blancardella, Phyllonorycter crataegella, Pieris spp., for example Pieris rapae, Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella (=Plutella maculipennis), Podesia spp., for example Podesia syringae, Prays spp., Prodenia spp., Protoparce spp., Pseudaletia spp., for example Pseudaletia unipuncta, Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., for example Schoenobius bipunctifer, Scirpophaga spp., for example Scirpophaga innotata, Scotia segetum, Sesamia spp., for example Sesamia inferens, Sparganothis spp., Spodoptera spp., for example Spodoptera eradiana, Spodoptera exigua, Spodoptera frugiperda, Spodoptera praefica, Stathmopoda spp., Stenoma spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thaumetopoea spp., Thermesia gemmatalis, Tinea cloacella, Tinea pellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzella, Trichoplusia spp., for example Trichoplusia ni, Tryporyza incertulas, Tuta absoluta, Virachola spp.; from the order of the Orthoptera or Saltatoria, for example Acheta domesticus, Dichroplus spp., Gryllotalpa spp., for example Gryllotalpa gryllotalpa, Hieroglyphus spp., Locusta spp., for example Locusta migratoria, Melanoplus spp., for example Melanoplus devastator, Paratlanticus ussuriensis, Schistocerca gregaria; from the order of the Phthiraptera, for example Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Phylloxera vastatrix, Phthirus pubis, Trichodectes spp.; from the order of the Psocoptera, for example Lepinotus spp., Liposcelis spp.; from the order of the Siphonaptera, for example, Ceratophyllus spp., Ctenocephalides spp., for example Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis; from the order of the Thysanoptera, for example Anaphothrips obscurus, Baliothrips biformis, Chaetanaphothrips leeuweni, Drepanothrips reuteri, Enneothrips flavens, Frankliniella spp., for example Frankliniella fusca, Frankliniella occidentalis, Frankliniella schultzei, Frankliniella tritici, Frankliniella vaccinii, Frankliniella williamsi, Haplothrips spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamomi, Thrips spp., for example Thrips palmi, Thrips tabaci; from the order of the Zygentoma (= Thysanura), for example Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class of the Symphyla, for example Scutigerella spp., for example Scutigerella immaculata; pests from the phylum of the Mollusca, for example from the class of the Bivalvia, for example Dreissena spp., and also from the class of the Gastropoda, for example Arion spp., for example Arion ater rufus, Biomphalaria spp., Bulinus spp., Deroceras spp., for example Deroceras laeve, Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp.; plant pests from the phylum of the Nematoda, i.e. phytoparasitic nematodes, in particular Aglenchus spp., for example Aglenchus agricola, Anguina spp., for example Anguina tritici, Aphelenchoides spp., for example Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., for example Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp., for example Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., for example Cacopaurus pestis, Criconemella spp., for example Criconemella curvata, Criconemella onoensis, Criconemella ornata, Criconemella rusium, Criconemella xenoplax (= Mesocriconema xenoplax), Criconemoides spp., for example Criconemoides ferniae, Criconemoides onoense, Criconemoides ornatum, Ditylenchus spp., for example Ditylenchus dipsaci, Dolichodorus spp., Globodera spp., for example Globodera pallida, Globodera rostochiensis, Helicotylenchus spp., for example Helicotylenchus dihystera, Hemicriconemoides spp., Hemicycliophora spp., Heterodera spp., for example Heterodera avenae, Heterodera glycines, Heterodera schachtii, Hirschmaniella spp., Hoplolaimus spp., Longidorus spp., for example Longidorus africanus, Meloidogyne spp., for example Meloidogyne chitwoodi, Meloidogyne fallax, Meloidogyne hapla, Meloidogyne incognita, Meloinema spp., Nacobbus spp., Neotylenchus spp., ., Paralongidorus spp., Paraphelenchus spp., Paratrichodorus spp., for example Paratrichodorus minor, Paratylenchus spp., Pratylenchus spp., for example Pratylenchus penetrans, Pseudohalenchus spp., Psilenchus spp., Punctodera spp., Quinisulcius spp., Radopholus spp., for example Radopholus citrophilus, Radopholus similis, Rotylenchulus spp., Rotylenchus spp., Scutellonema spp., Subanguina spp., Trichodorus spp., for example Trichodorus obtusus, Trichodorus primitivus, Tylenchorhynchus spp., for example Tylenchorhynchus annulatus, Tylenchulus spp., for example Tylenchulus semipenetrans, Xiphinema spp., for example Xiphinema index. The compounds of the formula (I) can optionally, at certain concentrations or application rates, also be used as herbicides, safeners, growth regulators or agents to improve plant properties, as microbicides or gametocides, for example as fungicides, antimycotics, bactericides, viricides (including agents against viroids) or as agents against MLO (mycoplasma-like organisms) and RLO (rickettsia-like organisms). If appropriate, they can also be used as intermediates or precursors for the synthesis of other active compounds. Formulations The present invention further relates to formulations, compositions and use forms comprising at least one compound of the formula (I) as defined anywhere supra. Such formulations and compositions are in particular prepared as pesticides, for example drench, drip and spray liquors, comprising at least one compound of the formula (I). Such formulations may further comprise at least one further compound selected from auxiliaries, excipients, solvents and/or additional pharmaceutically active agents. In some cases, the formulations or use forms comprise further pesticides and/or adjuvants which improve action, such as penetrants, e.g. vegetable oils, for example rapeseed oil, sunflower oil, mineral oils, for example paraffin oils, alkyl esters of vegetable fatty acids, for example rapeseed oil methyl ester or soya oil methyl ester, or alkanol alkoxylates and/or spreaders, for example alkylsiloxanes and/or salts, for example organic or inorganic ammonium or phosphonium salts, for example ammonium sulphate or diammonium hydrogenphosphate and/or retention promoters, for example dioctyl sulphosuccinate or hydroxypropyl guar polymers and/or humectants, for example glycerol and/or fertilizers, for example ammonium-, potassium- or phosphorus-containing fertilizers. Customary formulations are, for example, water-soluble liquids (SL), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS); these and further possible formulation types are described, for example, by Crop Life International and in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers – 173, prepared by the FAO/WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576. The formulations, in addition to one or more compounds of the formula (I), optionally comprise further agrochemically active compounds. These are preferably formulations or use forms which comprise auxiliaries, for example extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, biocides, thickeners and/or further auxiliaries, for example adjuvants. An adjuvant in this context is a component which enhances the biological effect of the formulation, without the component itself having any biological effect. Examples of adjuvants are agents which promote retention, spreading, attachment to the leaf surface or penetration. These formulations are prepared in a known way, for example by mixing the compounds of the formula (I) with auxiliaries such as, for example, extenders, solvents and/or solid carriers and/or other auxiliaries such as, for example, surfactants. The formulations are prepared either in suitable facilities or else before or during application. The auxiliaries used may be substances suitable for imparting special properties, such as certain physical, technical and/or biological properties, to the formulation of the compounds of the formula (I), or to the use forms prepared from these formulations (for example ready-to-use pesticides such as spray liquors or seed dressing products). Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), the esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide), the carbonates and the nitriles. If the extender used is water, it is also possible to employ, for example, organic solvents as auxiliary solvents. Essentially, suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example mineral oil fractions, mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide or dimethyl sulphoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, or nitriles such as acetonitrile or propanenitrile. In principle, it is possible to use all suitable solvents. Examples of suitable solvents are aromatic hydrocarbons, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons, such as chlorobenzene, chloroethylene or methylene chloride, aliphatic hydrocarbons, such as cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols, such as methanol, ethanol, isopropanol, butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethyl sulphoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, nitriles such as acetonitrile or propanenitrile, and also water. In principle, it is possible to use all suitable carriers. Useful carriers include especially: for example ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic materials such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and/or solid fertilizers. Mixtures of such carriers can likewise be used. Useful carriers for granules include: for example crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite, and synthetic granules of inorganic and organic meals, and also granules of organic material such as sawdust, paper, coconut shells, corn cobs and tobacco stalks. Liquefied gaseous extenders or solvents can also be used. Particularly suitable extenders or carriers are those which are gaseous at ambient temperature and under atmospheric pressure, for example aerosol propellant gases, such as halohydrocarbons, and also butane, propane, nitrogen and carbon dioxide. Examples of emulsifiers and/or foam-formers, dispersants or wetting agents with ionic or nonionic properties, or mixtures of these surfactants, are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyl taurates), isethionate derivatives, phosphoric esters of polyethoxylated alcohols or phenols, fatty esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, protein hydrolysates, lignosulphite waste liquors and methylcellulose. The presence of a surfactant is advantageous if one of the compounds of the formula (I) and/or one of the inert carriers is insoluble in water and when the application takes place in water. It is possible to use colorants such as inorganic pigments, for example iron oxide, titanium oxide and Prussian Blue, and organic dyes such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and nutrients and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc as further auxiliaries in the formulations and the use forms derived therefrom. Additional components may be stabilizers, such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability. Foam formers or antifoams may also be present. Tackifiers such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, or else natural phospholipids such as cephalins and lecithins and synthetic phospholipids may also be present as additional auxiliaries in the formulations and the use forms derived therefrom. Further possible auxiliaries are mineral and vegetable oils. Optionally, further auxiliaries may be present in the formulations and the use forms derived therefrom. Examples of such additives include fragrances, protective colloids, binders, adhesives, thickeners, thixotropic agents, penetrants, retention promoters, stabilizers, sequestrants, complexing agents, humectants, spreaders. In general, the compounds of the formula (I) can be combined with any solid or liquid additive commonly used for formulation purposes. Useful retention promoters include all those substances which reduce the dynamic surface tension, for example dioctyl sulphosuccinate, or increase the viscoelasticity, for example hydroxypropylguar polymers. Suitable penetrants in the present context are all those substances which are usually used for improving the penetration of agrochemical active compounds into plants. Penetrants are defined in this context by their ability to penetrate from the (generally aqueous) application liquor and/or from the spray coating into the cuticle of the plant and thereby increase the mobility of active compounds in the cuticle. The method described in the literature (Baur et al., 1997, Pesticide Science 51, 131-152) can be used to determine this property. Examples include alcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters, for example rapeseed oil methyl ester or soya oil methyl ester, fatty amine alkoxylates, for example tallowamine ethoxylate (15), or ammonium and/or phosphonium salts, for example ammonium sulphate or diammonium hydrogenphosphate. The formulations preferably comprise between 0.00000001 and 98% by weight of the compound of the formula (I) or, with particular preference, between 0.01% and 95% by weight of the compound of the formula (I), more preferably between 0.5% and 90% by weight of the compound of the formula (I), based on the weight of the formulation. The content of the compound of the formula (I) in the use forms prepared from the formulations (in particular pesticides) may vary within wide ranges. The concentration of the compound of the formula (I) in the use forms is usually between 0.00000001 and 95% by weight of the compound of the formula (I), preferably between 0.00001 and 1% by weight, based on the weight of the use form. The compounds are employed in a customary manner appropriate for the use forms. Mixtures The compounds of the formula (I) may also be employed as a mixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficial species, herbicides, fertilizers, bird repellents, phytotonics, sterilants, safeners, semiochemicals and/or plant growth regulators, in order thus, for example, to broaden the spectrum of action, to prolong the duration of action, to increase the rate of action, to prevent repulsion or prevent evolution of resistance. In addition, such active compound combinations may improve plant growth and/or tolerance to abiotic factors, for example high or low temperatures, to drought or to elevated water content or soil salinity. It is also possible to improve flowering and fruiting performance, optimize germination capacity and root development, facilitate harvesting and improve yields, influence maturation, improve the quality and/or the nutritional value of the harvested products, prolong storage life and/or improve the processability of the harvested products. Furthermore, the compounds of the formula (I) can be present in a mixture with other active compounds or semiochemicals such as attractants and/or bird repellants and/or plant activators and/or growth regulators and/or fertilizers. Likewise, the compounds of the formula (I) can be used to improve plant properties such as, for example, growth, yield and quality of the harvested material. In a particular embodiment according to the invention, the compounds of the formula (I) are present in formulations or the use forms prepared from these formulations in a mixture with further compounds, preferably those as described below. If one of the compounds mentioned below can occur in different tautomeric forms, these forms are also included even if not explicitly mentioned in each case. Further, all named mixing partners can, if their functional groups enable this, optionally form salts with suitable bases or acids. Insecticides/acaricides/nematicides The active compounds identified here by their common names are known and are described, for example, in the pesticide handbook (“The Pesticide Manual” 16th Ed., British Crop Protection Council 2012) or can be found on the Internet (e.g. http://www.alanwood.net/pesticides). The classification is based on the current IRAC Mode of Action Classification Scheme at the time of filing of this patent application. (1) Acetylcholinesterase (AChE) inhibitors, preferably carbamates selected from alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb, or organophosphates selected from acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl O-(methoxyaminothiophosphoryl) salicylate, isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos, monocrotophos, naled, omethoate, oxydemeton-methyl, parathion-methyl, phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim, pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos, pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos, tetrachlorvinphos, thiometon, triazophos, triclorfon and vamidothion. (2) GABA-gated chloride channel blockers, preferably cyclodiene-organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fiproles) selected from ethiprole and fipronil. (3) Sodium channel modulators, preferably pyrethroids selected from acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin s-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(1R)-trans-isomer], deltamethrin, empenthrin [(EZ)-(1R)-isomer], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, imiprothrin, kadethrin, momfluorothrin, permethrin, phenothrin [(1R)-trans-isomer], prallethrin, pyrethrins (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin [(1R)- isomer)], tralomethrin and transfluthrin or DDT or methoxychlor. (4) Nicotinic acetylcholine receptor (nAChR) competitive modulators, preferably neonicotinoids selected from acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam, or nicotine, or sulfoximines selected from sulfoxaflor, or butenolids selected from flupyradifurone, or mesoionics selected from triflumezopyrim. (5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators, preferably spinosyns selected from spinetoram and spinosad. (6) Glutamate-gated chloride channel (GluCl) allosteric modulators, preferably avermectins/milbemycins selected from abamectin, emamectin benzoate, lepimectin and milbemectin. (7) Juvenile hormone mimics, preferably juvenile hormone analogues selected from hydroprene, kinoprene and methoprene, or fenoxycarb or pyriproxyfen. (8) Miscellaneous non-specific (multi-site) inhibitors, preferably alkyl halides selected from methyl bromide and other alkyl halides, or chloropicrine or sulphuryl fluoride or borax or tartar emetic or methyl isocyanate generators selected from diazomet and metam. (9) Chordotonal organ TRPV channel modulators selected from pymetrozine and pyrifluquinazone. (10) Mite growth inhibitors selected from clofentezine, hexythiazox, diflovidazin and etoxazole. (11) Microbial disruptors of the insect gut membrane selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis, and B.t. plant proteins selected from Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb and Cry34Ab1/35Ab1. (12) Inhibitors of mitochondrial ATP synthase, preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotin, cyhexatin and fenbutatin oxide, or propargite or tetradifon. (13) Uncouplers of oxidative phosphorylation via disruption of the proton gradient selected from chlorfenapyr, DNOC and sulfluramid. (14) Nicotinic acetylcholine receptor channel blockers selected from bensultap, cartap hydrochloride, thiocylam and thiosultap-sodium. (15) Inhibitors of chitin biosynthesis, type 0, selected from bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron. (16) Inhibitors of chitin biosynthesis, type 1 selected from buprofezin. (17) Moulting disruptor (in particular for Diptera, i.e. dipterans) selected from cyromazine. (18) Ecdysone receptor agonists selected from chromafenozide, halofenozide, methoxyfenozide and tebufenozide. (19) Octopamine receptor agonists selected from amitraz. (20) Mitochondrial complex III electron transport inhibitors selected from hydramethylnone, acequinocyl and fluacrypyrim. (21) Mitochondrial complex I electron transport inhibitors, preferably METI acaricides selected from fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad and tolfenpyrad, or rotenone (Derris). (22) Voltage-dependent sodium channel blockers selected from indoxacarb and metaflumizone. (23) Inhibitors of acetyl CoA carboxylase, preferably tetronic and tetramic acid derivatives selected from spirodiclofen, spiromesifen and spirotetramat. (24) Mitochondrial complex IV electron transport inhibitors, preferably phosphines selected from aluminium phosphide, calcium phosphide, phosphine and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide and sodium cyanide. (25) Mitochondrial complex II electron transport inhibitors, preferably beta-ketonitrile derivatives selected from cyenopyrafen and cyflumetofen, and carboxanilides selected from pyflubumide. (28) Ryanodine receptor modulators, preferably diamides selected from chlorantraniliprole, cyantraniliprole and flubendiamide. (29) Chordotonal organ Modulators (with undefined target site) selected from flonicamid. (30) further active compounds selected from Acynonapyr, Afidopyropen, Afoxolaner, Azadirachtin, Benclothiaz, Benzoximate, Benzpyrimoxan, Bifenazate, Broflanilide, Bromopropylate, Chinomethionat, Chloroprallethrin, Cryolite, Cyclaniliprole, Cycloxaprid, Cyhalodiamide, Dicloromezotiaz, Dicofol, Dimpropyridaz, epsilon-Metofluthrin, epsilon-Momfluthrin, Flometoquin, Fluazaindolizine, Fluensulfone, Flufenerim, Flufenoxystrobin, Flufiprole, Fluhexafon, Fluopyram, Flupyrimin, Fluralaner, Fluxametamide, Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione, Isocycloseram, kappa- Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin, Oxazosulfyl, Paichongding, Pyridalyl, Pyrifluquinazon, Pyriminostrobin, Spirobudiclofen, Spiropidion, Tetramethylfluthrin, Tetraniliprole, Tetrachlorantraniliprole, Tigolaner, Tioxazafen, Thiofluoximate iodomethane; furthermore preparations based on Bacillus firmus (I-1582, BioNeem, Votivo), and also the following compounds: 1-{2-fluoro-4- methyl-5-[(2,2,2-trifluoroethyl)sulphinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine (known from WO2006/043635) (CAS 885026-50-6), {1'-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]-5- fluorospiro[indol-3,4'-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methanone (known from WO2003/106457) (CAS 637360-23-7), 2-chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1- yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide (known from WO2006/003494) (CAS 872999-66-1), 3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2- one (known from WO 2010052161) (CAS 1225292-17-0), 3-(4-chloro-2,6-dimethylphenyl)-8-methoxy- 2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl ethyl carbonate (known from EP2647626) (CAS 1440516-42-6) , 4-(but-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine (known from WO2004/099160) (CAS 792914-58-0), PF1364 (known from JP2010/018586) (CAS 1204776-60-2), (3E)-3-[1-[(6-chloro- 3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoro-propan-2-one (known from WO2013/144213) (CAS 1461743-15-6), , N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(pentafluoroethyl)-4- (trifluoromethyl)-1H-pyrazole-5-carboxamide (known from WO2010/051926) (CAS 1226889-14-0), 5- bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3- carboxamide (known from CN103232431) (CAS 1449220-44-3), 4-[5-(3,5-dichlorophenyl)-4,5-dihydro- 5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)-benzamide, 4-[5-(3,5- dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(trans-1-oxido-3-thietanyl)- benzamide and 4-[(5S)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl- N-(cis-1-oxido-3-thietanyl)benzamide (known from WO 2013/050317 A1) (CAS 1332628-83-7), N-[3- chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide, (+)-N- [3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide and (-)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]- propanamide (known from WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 A1) (CAS 1477923-37-7), 5-[[(2E)-3-chloro-2-propen-1-yl]amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4- [(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile (known from CN 101337937 A) (CAS 1105672- 77-2), 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)thioxomethyl]phenyl]-1-(3-chloro-2-pyridinyl)- 1H-pyrazole-5-carboxamide, (Liudaibenjiaxuanan, known from CN 103109816 A) (CAS 1232543-85-9); N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3- (fluoromethoxy)-1H-Pyrazole-5-carboxamide (known from WO 2012/034403 A1) (CAS 1268277-22-0), N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H- pyrazole-5-carboxamide (known from WO 2011/085575 A1) (CAS 1233882-22-8), 4-[3-[2,6-dichloro-4- [(3,3-dichloro-2-propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)-pyrimidine (known from CN 101337940 A) (CAS 1108184-52-6); (2E)- and 2(Z)-2-[2-(4-cyanophenyl)-1-[3- (trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide (known from CN 101715774 A) (CAS 1232543-85-9); 3-(2,2-dichloroethenyl)-2,2-dimethyl-4-(1H- benzimidazol-2-yl)phenyl-cyclopropanecarboxylic acid ester (known from CN 103524422 A) (CAS 1542271-46-4); (4aS)-7-chloro-2,5-dihydro-2-[[(methoxycarbonyl)[4-[(trifluoromethyl)thio]phenyl] amino]carbonyl]-indeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylic acid methyl ester (known from CN 102391261 A) (CAS 1370358-69-2); 6-deoxy-3-O-ethyl-2,4-di-O-methyl-, 1-[N-[4-[1-[4-(1,1,2,2,2- pentafluoroethoxy)phenyl]-1H-1,2,4-triazol-3-yl]phenyl]carbamate]-α-L-mannopyranose (known from US 2014/0275503 A1) (CAS 1181213-14-8); 8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3- (6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1 ]octane (CAS 1253850-56-4), (8-anti)-8-(2- cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza- bicyclo[3.2.1 ]octane (CAS 933798-27-7), (8-syn)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy) -3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1 ]octane (known from WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8), N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3- [(3,3,3-trifluoropropyl)thio]-propanamide (known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) and N-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl]-3- bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide (known from CN 103265527 A) (CAS 1452877-50-7), 5-(1,3-dioxan-2-yl)-4-[[4-(trifluoromethyl)phenyl]methoxy]-pyrimidine (known from WO 2013/115391 A1) (CAS 1449021-97-9), 3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8- diazaspiro[4.5]decane-2,4-dione (known from WO 2014/187846 A1) (CAS 1638765-58-8), 3-(4-chloro- 2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carbonic acid ethyl ester (known from WO 2010/066780 A1, WO 2011151146 A1) (CAS 1229023-00-0), 4-[(5S)-5-(3,5- Dichloro-4-fluorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[(4R)-2-ethyl-3-oxo-4- isoxazolidinyl]-2-methyl-benzamide (bekannt aus WO 2011/067272, WO2013/050302) (CAS 1309959- 62-3). Fungicides The active ingredients specified herein by their Common Name are known and described, for example, in The Pesticide Manual (16th Ed.British Crop Protection Council) or can be searched in the internet (e.g. www.alanwood.net/pesticides). All named fungicidal mixing partners of the classes (1) to (15) can, if their functional groups enable this, optionally form salts with suitable bases or acids. All named mixing partners of the classes (1) to (15) can include tautomeric forms, where applicable. 1) Inhibitors of the ergosterol biosynthesis, for example (1.001) cyproconazole, (1.002) difenoconazole, (1.003) epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalil, (1.011) imazalil sulfate, (1.012) ipconazole, (1.013) metconazole, (1.014) myclobutanil, (1.015) paclobutrazol, (1.016) prochloraz, (1.017) propiconazole, (1.018) prothioconazole, (1.019) Pyrisoxazole, (1.020) spiroxamine, (1.021) tebuconazole, (1.022) tetraconazole, (1.023) triadimenol, (1.024) tridemorph, (1.025) triticonazole, (1.026) (1R,2S,5S)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)- cyclopentanol, (1.027) (1S,2R,5R)-5-(4-chlorobenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4-triazol-1- ylmethyl)cyclopentanol, (1.028) (2R)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2-dichlorocyclopropyl]-1-(1H- 1,2,4-triazol-1-yl)butan-2-ol, (1.029) (2R)-2-(1-chlorocyclopropyl)-4-[(1S)-2,2-dichlorocyclopropyl]-1- (1H-1,2,4-triazol-1-yl)butan-2-ol, (1.030) (2R)-2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1- (1H-1,2,4-triazol-1-yl)propan-2-ol, (1.031) (2S)-2-(1-chlorocyclopropyl)-4-[(1R)-2,2- dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.032) (2S)-2-(1-chlorocyclopropyl)-4-[(1S)- 2,2-dichlorocyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.033) (2S)-2-[4-(4-chlorophenoxy)-2- (trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.034) (R)-[3-(4-chloro-2-fluorophenyl)- 5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035) (S)-[3-(4-chloro-2- fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.036) [3-(4-chloro-2- fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.037) 1-({(2R,4S)-2-[2- chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazole, (1.038) 1- ({(2S,4S)-2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4- triazole, (1.039) 1-{[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.040) 1-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H- 1,2,4-triazol-5-yl thiocyanate, (1.041) 1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran- 2-yl]methyl}-1H-1,2,4-triazol-5-yl thiocyanate, (1.042) 2-[(2R,4R,5R)-1-(2,4-dichlorophenyl)-5- hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.043) 2-[(2R,4R,5S)-1- (2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.044) 2-[(2R,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H- 1,2,4-triazole-3-thione, (1.045) 2-[(2R,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan- 4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.046) 2-[(2S,4R,5R)-1-(2,4-dichlorophenyl)-5-hydroxy- 2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.047) 2-[(2S,4R,5S)-1-(2,4- dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.048) 2-[(2S,4S,5R)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4- triazole-3-thione, (1.049) 2-[(2S,4S,5S)-1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]- 2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.050) 2-[1-(2,4-dichlorophenyl)-5-hydroxy-2,6,6- trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.051) 2-[2-chloro-4-(2,4- dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.052) 2-[2-chloro-4-(4- chlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.053) 2-[4-(4-chlorophenoxy)-2- (trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (1.054) 2-[4-(4-chlorophenoxy)-2- (trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol, (1.055) Mefentrifluconazole, (1.056) 2- {[3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3- thione, (1.057) 2-{[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-2,4- dihydro-3H-1,2,4-triazole-3-thione, (1.058) 2-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)- oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.059) 5-(4-chlorobenzyl)-2-(chloro- methyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.060) 5-(allylsulfanyl)-1-{[3-(2- chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.061) 5-(allylsulfanyl)-1- {[rel(2R,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole, (1.062) 5-(allylsulfanyl)-1-{[rel(2R,3S)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)oxiran-2-yl]methyl}-1H- 1,2,4-triazole, (1.063) N'-(2,5-dimethyl-4-{[3-(1,1,2,2-tetrafluoroethoxy)phenyl]sulfanyl}phenyl)-N- ethyl-N-methylimidoformamide, (1.064) N'-(2,5-dimethyl-4-{[3-(2,2,2- trifluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.065) N'-(2,5-dimethyl-4- {[3-(2,2,3,3-tetrafluoropropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.066) N'- (2,5-dimethyl-4-{[3-(pentafluoroethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamide, (1.067) N'-(2,5-dimethyl-4-{3-[(1,1,2,2-tetrafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N- methylimidoformamide, (1.068) N'-(2,5-dimethyl-4-{3-[(2,2,2-trifluoroethyl)sulfanyl]phenoxy}phenyl)- N-ethyl-N-methylimidoformamide, (1.069) N'-(2,5-dimethyl-4-{3-[(2,2,3,3- tetrafluoropropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.070) N'-(2,5- dimethyl-4-{3-[(pentafluoroethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamide, (1.071) N'-(2,5-dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamide, (1.072) N'-(4-{[3- (difluoromethoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.073) N'- (4-{3-[(difluoromethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, (1.074) N'-[5-bromo-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin-3-yl]-N-ethyl-N-methylimido- formamide, (1.075) N'-{4-[(4,5-dichloro-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl-N- methylimidoformamide, (1.076) N'-{5-bromo-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3- yl}-N-ethyl-N-methylimidoformamide, (1.077) N'-{5-bromo-6-[(1S)-1-(3,5-difluorophenyl)ethoxy]-2- methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.078) N'-{5-bromo-6-[(cis-4- isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.079) N'-{5- bromo-6-[(trans-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamide, (1.080) N'-{5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N- methylimidoformamide, (1.081) Ipfentrifluconazole. 2) Inhibitors of the respiratory chain at complex I or II, for example (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad, (2.008) furametpyr, (2.009) Isofetamid, (2.010) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.020) Pyraziflumid, (2.021) sedaxane, (2.022) 1,3-dimethyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.023) 1,3- dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.024) 1,3- dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole-4-carboxamide, (2.025) 1- methyl-3-(trifluoromethyl)-N-[2'-(trifluoromethyl)biphenyl-2-yl]-1H-pyrazole-4-carboxamide, (2.026) 2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide, (2.027) 3- (difluoromethyl)-1-methyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.028) 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazole- 4-carboxamide, (2.029) 3-(difluoromethyl)-1-methyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4- yl]-1H-pyrazole-4-carboxamide, (2.030) Fluindapyr, (2.031) 3-(difluoromethyl)-N-[(3R)-7-fluoro-1,1,3- trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4-carboxamide, (2.032) 3- (difluoromethyl)-N-[(3S)-7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazole-4- carboxamide, (2.033) 5,8-difluoro-N-[2-(2-fluoro-4-{[4-(trifluoromethyl)pyridin-2-yl]oxy}- phenyl)ethyl]quinazolin-4-amine, (2.034) N-(2-cyclopentyl-5-fluorobenzyl)-N-cyclopropyl-3- (difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.035) N-(2-tert-butyl-5- methylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.036) N-(2-tert-butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4- carboxamide, (2.037) N-(5-chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl- 1H-pyrazole-4-carboxamide, (2.038) isoflucypram, (2.039) N-[(1R,4S)-9-(dichloromethylene)-1,2,3,4- tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.040) N-[(1S,4R)-9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoro- methyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.041) N-[1-(2,4-dichlorophenyl)-1-methoxypropan-2- yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.042) N-[2-chloro-6- (trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4- carboxamide, (2.043) N-[3-chloro-2-fluoro-6-(trifluoromethyl)benzyl]-N-cyclopropyl-3- (difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.044) N-[5-chloro-2- (trifluoromethyl)benzyl]-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4- carboxamide, (2.045) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-N-[5-methyl-2- (trifluoromethyl)benzyl]-1H-pyrazole-4-carboxamide, (2.046) N-cyclopropyl-3-(difluoromethyl)-5- fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.047) N-cyclopropyl-3- (difluoromethyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.048) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4- carbothioamide, (2.049) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl- 1H-pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(5-fluoro-2- isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide, (2.051) N-cyclopropyl-3-(difluoromethyl)-N- (2-ethyl-4,5-dimethylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052) N-cyclopropyl-3- (difluoromethyl)-N-(2-ethyl-5-fluorobenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.053) N- cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4- carboxamide, (2.054) N-cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3-(difluoromethyl)-5-fluoro-1- methyl-1H-pyrazole-4-carboxamide, (2.055) N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3- (difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.056) N-cyclopropyl-N-(2- cyclopropylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.057) pyrapropoyne. 3) Inhibitors of the respiratory chain at complex III, for example (3.001) ametoctradin, (3.002) amisulbrom, (3.003) azoxystrobin, (3.004) coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamid, (3.007) dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010) fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-fluoro-2- phenylvinyl]oxy}phenyl)ethylidene]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamide, (3.022) (2E,3Z)-5-{[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3- enamide, (3.023) (2R)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.024) (2S)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamide, (3.025) (3S,6S,7R,8R)-8-benzyl-3-[({3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2-yl}carbonyl)amino]-6- methyl-4,9-dioxo-1,5-dioxonan-7-yl 2-methylpropanoate, (3.026) mandestrobin, (3.027) N-(3-ethyl- 3,5,5-trimethylcyclohexyl)-3-formamido-2-hydroxybenzamide, (3.028) (2E,3Z)-5-{[1-(4-chloro-2- fluorophenyl)-1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamide, (3.029) methyl {5-[3-(2,4-dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl}carbamate, (3.030) metyltetraprole, (3.031) florylpicoxamid. 4) Inhibitors of the mitosis and cell division, for example (4.001) carbendazim, (4.002) diethofencarb, (4.003) ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate- methyl, (4.008) zoxamide, (4.009) 3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenylpyridazine, (4.010) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, (4.011) 3-chloro-5-(6- chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine, (4.012) 4-(2-bromo-4-fluorophenyl)- N-(2,6-difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.013) 4-(2-bromo-4-fluorophenyl)-N-(2- bromo-6-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.014) 4-(2-bromo-4-fluorophenyl)-N-(2- bromophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.015) 4-(2-bromo-4-fluorophenyl)-N-(2-chloro-6- fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.016) 4-(2-bromo-4-fluorophenyl)-N-(2- chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.017) 4-(2-bromo-4-fluorophenyl)-N-(2- fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.018) 4-(2-chloro-4-fluorophenyl)-N-(2,6- difluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.019) 4-(2-chloro-4-fluorophenyl)-N-(2-chloro-6- fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.020) 4-(2-chloro-4-fluorophenyl)-N-(2- chlorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.021) 4-(2-chloro-4-fluorophenyl)-N-(2- fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.022) 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6- dimethylpyridazine, (4.023) N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H- pyrazol-5-amine, (4.024) N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5- amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol- 5-amine. 5) Compounds capable to have a multisite action, for example (5.001) bordeaux mixture, (5.002) captafol, (5.003) captan, (5.004) chlorothalonil, (5.005) copper hydroxide, (5.006) copper naphthenate, (5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper(2+) sulfate, (5.010) dithianon, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) metiram, (5.016) metiram zinc, (5.017) oxine- copper, (5.018) propineb, (5.019) sulfur and sulfur preparations including calcium polysulfide, (5.020) thiram, (5.021) zineb, (5.022) ziram, (5.023) 6-ethyl-5,7-dioxo-6,7-dihydro-5H- pyrrolo[3',4':5,6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile. 6) Compounds capable to induce a host defence, for example (6.001) acibenzolar-S-methyl, (6.002) isotianil, (6.003) probenazole, (6.004) tiadinil. 7) Inhibitors of the amino acid and/or protein biosynthesis, for example (7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycin hydrochloride hydrate, (7.004) oxytetracycline, (7.005) pyrimethanil, (7.006) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline. 8) Inhibitors of the ATP production, for example (8.001) silthiofam. 9) Inhibitors of the cell wall synthesis, for example (9.001) benthiavalicarb, (9.002) dimethomorph, (9.003) flumorph, (9.004) iprovalicarb, (9.005) mandipropamid, (9.006) pyrimorph, (9.007) valifenalate, (9.008) (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (9.009) (2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one. 10) Inhibitors of the lipid and membrane synthesis, for example (10.001) propamocarb, (10.002) propamocarb hydrochloride, (10.003) tolclofos-methyl. 11) Inhibitors of the melanin biosynthesis, for example (11.001) tricyclazole, (11.002) 2,2,2-trifluoroethyl {3-methyl-1-[(4-methylbenzoyl)amino]butan-2-yl}carbamate. 12) Inhibitors of the nucleic acid synthesis, for example (12.001) benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam). 13) Inhibitors of the signal transduction, for example (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazid, (13.005) quinoxyfen, (13.006) vinclozolin. 14) Compounds capable to act as an uncoupler, for example (14.001) fluazinam, (14.002) meptyldinocap. 15) Further compounds, for example (15.001) Abscisic acid, (15.002) benthiazole, (15.003) bethoxazin, (15.004) capsimycin, (15.005) carvone, (15.006) chinomethionat, (15.007) cufraneb, (15.008) cyflufenamid, (15.009) cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl- aluminium, (15.013) fosetyl-calcium, (15.014) fosetyl-sodium, (15.015) methyl isothiocyanate, (15.016) metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019) nickel dimethyldithiocarbamate, (15.020) nitrothal-isopropyl, (15.021) oxamocarb, (15.022) oxathiapiprolin, (15.023) oxyfenthiin, (15.024) pentachlorophenol and salts, (15.025) phosphorous acid and its salts, (15.026) propamocarb- fosetylate, (15.027) pyriofenone (chlazafenone), (15.028) tebufloquin, (15.029) tecloftalam, (15.030) tolnifanide, (15.031) 1-(4-{4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2- yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.032) 1-(4-{4-[(5S)-5- (2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3- (trifluoromethyl)-1H-pyrazol-1-yl]ethanone, (15.033) 2-(6-benzylpyridin-2-yl)quinazoline, (15.034) dipymetitrone, (15.035) 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-yn-1- yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.036) 2-[3,5- bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro- 1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone, (15.037) 2-[3,5-bis(difluoromethyl)-1H- pyrazol-1-yl]-1-[4-(4-{5-[2-fluoro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3- thiazol-2-yl)piperidin-1-yl]ethanone, (15.038) 2-[6-(3-fluoro-4-methoxyphenyl)-5-methylpyridin-2- yl]quinazoline, (15.039) 2-{(5R)-3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4- yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.040) 2-{(5S)-3- [2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro- 1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.041) Ipflufenoquin, (15.042) 2-{2-fluoro-6-[(8- fluoro-2-methylquinolin-3-yl)oxy]phenyl}propan-2-ol, (15.043) 2-{3-[2-(1-{[3,5-bis(difluoromethyl)- 1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenyl methanesulfonate, (15.044) 2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4- yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl methanesulfonate, (15.045) 2-phenylphenol and salts, (15.046) 3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline, (15.047) quinofumelin, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin- 2(1H)-one), (15.049) 4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (15.050) 5-amino-1,3,4-thiadiazole- 2-thiol, (15.051) 5-chloro-N'-phenyl-N'-(prop-2-yn-1-yl)thiophene-2-sulfonohydrazide, (15.052) 5- fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, (15.053) 5-fluoro-2-[(4-methylbenzyl)oxy]pyrimidin- 4-amine, (15.054) 9-fluoro-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4-benzoxazepine, (15.055) but- 3-yn-1-yl {6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2- yl}carbamate, (15.056) ethyl (2Z)-3-amino-2-cyano-3-phenylacrylate, (15.057) phenazine-1-carboxylic acid, (15.058) propyl 3,4,5-trihydroxybenzoate, (15.059) quinolin-8-ol, (15.060) quinolin-8-ol sulfate (2:1), (15.061) tert-butyl {6-[({[(1-methyl-1H-tetrazol-5- yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (15.062) 5-fluoro-4-imino-3-methyl- 1-[(4-methylphenyl)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one, (15.063) aminopyrifen. Biological pesticides as mixing components The compounds of the formula (I) can be combined with biological pesticides. Biological pesticides comprise in particular bacteria, fungi, yeasts, plant extracts and products formed by microorganisms, including proteins and secondary metabolites. Biological pesticides comprise bacteria such as spore-forming bacteria, root-colonising bacteria and bacteria which act as biological insecticides, fungicides or nematicides. Examples of such bacteria which are employed or can be used as biological pesticides are: Bacillus amyloliquefaciens, strain FZB42 (DSM 231179), or Bacillus cereus, in particular B. cereus strain CNCM I-1562 or Bacillus firmus, strain I-1582 (Accession number CNCM I-1582) or Bacillus pumilus, in particular strain GB34 (Accession No. ATCC 700814) and strain QST2808 (Accession No. NRRL B- 30087), or Bacillus subtilis, in particular strain GB03 (Accession No. ATCC SD-1397), or Bacillus subtilis strain QST713 (Accession No. NRRL B-21661) or Bacillus subtilis strain OST 30002 (Accession No. NRRL B-50421) Bacillus thuringiensis, in particular B. thuringiensis subspecies israelensis (serotype H- 14), strain AM65-52 (Accession No. ATCC 1276), or B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), or B. thuringiensis subsp. kurstaki strain HD-1, or B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp. (Rotylenchulus reniformis nematode)-PR3 (Accession Number ATCC SD-5834), Streptomyces microflavus strain AQ6121 (= QRD 31.013, NRRL B-50550), Streptomyces galbus strain AQ 6047 (Acession Number NRRL 30232). Examples of fungi and yeasts which are employed or can be used as biological pesticides are: Beauveria bassiana, in particular strain ATCC 74040, Coniothyrium minitans, in particular strain CON/M/91-8 (Accession No. DSM-9660), Lecanicillium spp., in particular strain HRO LEC 12, Lecanicillium lecanii, (formerly known as Verticillium lecanii), in particular strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884/ ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (now: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No. ATCC 20874), Paecilomyces lilacinus, in particular P. lilacinus strain 251 (AGAL 89/030550), Talaromyces flavus, in particular strain V117b, Trichoderma atroviride, in particular strain SC1 (Accession Number CBS 122089), Trichoderma harzianum, in particular T. harzianum rifai T39. (Accession Number CNCM I-952). Examples of viruses which are employed or can be used as biological pesticides are: Adoxophyes orana (summer fruit tortrix) granulosis virus (GV), Cydia pomonella (codling moth) granulosis virus (GV), Helicoverpa armigera (cotton bollworm) nuclear polyhedrosis virus (NPV), Spodoptera exigua (beet armyworm) mNPV, Spodoptera frugiperda (fall armyworm) mNPV, Spodoptera littoralis (African cotton leafworm) NPV. Also included are bacteria and fungi which are added as 'inoculant' to plants or plant parts or plant organs and which, by virtue of their particular properties, promote plant growth and plant health. Examples which may be mentioned are: Agrobacterium spp., Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., in particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., or Gigaspora monosporum, Glomus spp., Laccaria spp., Lactobacillus buchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp., Rhizobium spp., in particular Rhizobium trifolii, Rhizopogon spp., Scleroderma spp., Suillus spp., Streptomyces spp. Examples of plant extracts and products formed by microorganisms including proteins and secondary metabolites which are employed or can be used as biological pesticides are: Allium sativum, Artemisia absinthium, azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodium anthelminticum, chitin, Armour-Zen, Dryopteris filix-mas, Equisetum arvense, Fortune Aza, Fungastop, Heads Up (Chenopodium quinoa saponin extract), Pyrethrum/Pyrethrins, Quassia amara, Quercus, Quillaja, Regalia, "Requiem ™ Insecticide", rotenone, ryania/ryanodine, Symphytum officinale, Tanacetum vulgare, thymol, Triact 70, TriCon, Tropaeulum majus, Urtica dioica, Veratrin, Viscum album, Brassicaceae extract, in particular oilseed rape powder or mustard powder. Safener as mixing components The compounds of the formula (I) can be combined with safeners such as, for example, benoxacor, cloquintocet (-mexyl), cyometrinil, cyprosulfamide, dichlormid, fenchlorazole (-ethyl), fenclorim, flurazole, fluxofenim, furilazole, isoxadifen (-ethyl), mefenpyr (-diethyl), naphthalic anhydride, oxabetrinil, 2-methoxy-N-({4-[(methylcarbamoyl)amino]phenyl}sulphonyl)benzamide (CAS 129531- 12-0), 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (CAS 71526-07-3), 2,2,5-trimethyl-3- (dichloroacetyl)-1,3-oxazolidine (CAS 52836-31-4). Plants and plant parts All plants and plant parts can be treated in accordance with the invention. Here, plants are to be understood to mean all plants and plant parts such as wanted and unwanted wild plants or crop plants (including naturally occurring crop plants), for example cereals (wheat, rice, triticale, barley, rye, oats), maize, soya bean, potato, sugar beet, sugar cane, tomatoes, pepper, cucumber, melon, carrot, watermelon, onion, lettuce, spinach, leek, beans, Brassica oleracea (e.g. cabbage) and other vegetable species, cotton, tobacco, oilseed rape, and also fruit plants (with the fruits apples, pears, citrus fruits and grapevines). Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or cannot be protected by varietal property rights. Plants should be understood to mean all developmental stages, such as seeds, seedlings, young (immature) plants up to mature plants. Plant parts should be understood to mean all parts and organs of the plants above and below ground, such as shoot, leaf, flower and root, examples given being leaves, needles, stalks, stems, flowers, fruit bodies, fruits and seeds, and also tubers, roots and rhizomes. Parts of plants also include harvested plants or harvested plant parts and vegetative and generative propagation material, for example seedlings, tubers, rhizomes, cuttings and seeds. Treatment according to the invention of the plants and plant parts with the compounds of the formula (I) is carried out directly or by allowing the compounds to act on the surroundings, environment or storage space by the customary treatment methods, for example by immersion, spraying, evaporation, fogging, scattering, painting on, injection and, in the case of propagation material, in particular in the case of seeds, also by applying one or more coats. As already mentioned above, it is possible to treat all plants and their parts according to the invention. In a preferred embodiment, wild plant species and plant cultivars, or those obtained by conventional biological breeding methods, such as crossing or protoplast fusion, and also parts thereof, are treated. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering methods, if appropriate in combination with conventional methods (genetically modified organisms), and parts thereof are treated. The term “parts” or “parts of plants” or “plant parts” has been explained above. The invention is used with particular preference to treat plants of the respective commercially customary cultivars or those that are in use. Plant cultivars are to be understood as meaning plants having new properties ("traits") and which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. They can be cultivars, varieties, bio- or genotypes. Transgenic plant, seed treatment and integration events The transgenic plants or plant cultivars (those obtained by genetic engineering) which are to be treated with preference in accordance with the invention include all plants which, through the genetic modification, received genetic material which imparts particular advantageous useful properties ("traits") to these plants. Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to levels of water or soil salinity, enhanced flowering performance, easier harvesting, accelerated ripening, higher yields, higher quality and/or a higher nutritional value of the harvested products, better storage life and/or processability of the harvested products. Further and particularly emphasized examples of such properties are increased resistance of the plants against animal and microbial pests, such as against insects, arachnids, nematodes, mites, slugs and snails owing, for example, to toxins formed in the plants, in particular those formed in the plants by the genetic material from Bacillus thuringiensis (for example by the genes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9c Cry2Ab, Cry3Bb and CryIF and also combinations thereof), furthermore increased resistance of the plants against phytopathogenic fungi, bacteria and/or viruses owing, for example, to systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and also resistance genes and correspondingly expressed proteins and toxins, and also increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulphonylureas, glyphosate or phosphinothricin (for example the "PAT" gene). The genes which impart the desired traits in question may also be present in combinations with one another in the transgenic plants. Examples of transgenic plants which may be mentioned are the important crop plants, such as cereals (wheat, rice, triticale, barley, rye, oats), maize, soya beans, potatoes, sugar beet, sugar cane, tomatoes, peas and other types of vegetable, cotton, tobacco, oilseed rape and also fruit plants (with the fruits apples, pears, citrus fruits and grapes), with particular emphasis being given to maize, soya beans, wheat, rice, potatoes, cotton, sugar cane, tobacco and oilseed rape. Traits which are particularly emphasized are the increased resistance of the plants to insects, arachnids, nematodes and slugs and snails. Crop protection – types of treatment The treatment of the plants and plant parts with the compounds of the formula (I) is carried out directly or by action on their surroundings, habitat or storage space using customary treatment methods, for example by dipping, spraying, atomizing, irrigating, evaporating, dusting, fogging, broadcasting, foaming, painting, spreading-on, injecting, watering (drenching), drip irrigating and, in the case of propagation material, in particular in the case of seed, furthermore as a powder for dry seed treatment, a solution for liquid seed treatment, a water-soluble powder for slurry treatment, by incrusting, by coating with one or more coats, etc. It is furthermore possible to apply the compounds of the formula (I) by the ultra-low volume method or to inject the application form or the compound of the formula (I) itself into the soil. A preferred direct treatment of the plants is foliar application, i.e. the compounds of the formula (I) are applied to the foliage, where treatment frequency and the application rate should be adjusted according to the level of infestation with the pest in question. In the case of systemically active compounds, the compounds of the formula (I) also access the plants via the root system. The plants are then treated by the action of the compounds of the formula (I) on the habitat of the plant. This may be done, for example, by drenching, or by mixing into the soil or the nutrient solution, i.e. the locus of the plant (e.g. soil or hydroponic systems) is impregnated with a liquid form of the compounds of the formula (I), or by soil application, i.e. the compounds of the formula (I) according to the invention are introduced in solid form (e.g. in the form of granules) into the locus of the plants, or by drip application (often also referred to as "chemigation"), i.e. the liquid application of the compounds of the formula (I) according to the invention from surface or sub-surface driplines over a certain period of time together with varying amounts of water at defined locations in the vicinity of the plants. In the case of paddy rice crops, this can also be done by metering the compound of the formula (I) in a solid application form (for example as granules) into a flooded paddy field. Treatment of seed The control of animal pests by treating the seed of plants has been known for a long time and is the subject of continuous improvements. However, the treatment of seed entails a series of problems which cannot always be solved in a satisfactory manner. Thus, it is desirable to develop methods for protecting the seed and the germinating plant which dispense with, or at least reduce considerably, the additional application of pesticides during storage, after sowing or after emergence of the plants. It is furthermore desirable to optimize the amount of active compound employed in such a way as to provide optimum protection for the seed and the germinating plant from attack by animal pests, but without damaging the plant itself by the active compound employed. In particular, methods for the treatment of seed should also take into consideration the intrinsic insecticidal or nematicidal properties of pest-resistant or -tolerant transgenic plants in order to achieve optimum protection of the seed and also the germinating plant with a minimum of pesticides being employed. The present invention therefore in particular also relates to a method for the protection of seed and germinating plants, from attack by pests, by treating the seed with one of the compounds of the formula (I). The method according to the invention for protecting seed and germinating plants against attack by pests furthermore comprises a method where the seed is treated simultaneously in one operation or sequentially with a compound of the formula (I) and a mixing component. It also comprises a method where the seed is treated at different times with a compound of the formula (I) and a mixing component. The invention likewise relates to the use of the compounds of the formula (I) for the treatment of seed for protecting the seed and the resulting plant from animal pests. Furthermore, the invention relates to seed which has been treated with a compound of the formula (I) according to the invention so as to afford protection from animal pests. The invention also relates to seed which has been treated simultaneously with a compound of the formula (I) and a mixing component. The invention furthermore relates to seed which has been treated at different times with a compound of the formula (I) and a mixing component. In the case of seed which has been treated at different points in time with a compound of the formula (I) and a mixing component, the individual substances may be present on the seed in different layers. Here, the layers comprising a compound of the formula (I) and mixing components may optionally be separated by an intermediate layer. The invention also relates to seed where a compound of the formula (I) and a mixing component have been applied as component of a coating or as a further layer or further layers in addition to a coating. Furthermore, the invention relates to seed which, after the treatment with a compound of the formula (I), is subjected to a film-coating process to prevent dust abrasion on the seed. One of the advantages encountered with a systemically acting compound of the formula (I) is the fact that, by treating the seed, not only the seed itself but also the plants resulting therefrom are, after emergence, protected against animal pests. In this manner, the immediate treatment of the crop at the time of sowing or shortly thereafter can be dispensed with. It has to be considered a further advantage that by treatment of the seed with a compound of the formula (I), germination and emergence of the treated seed may be enhanced. It is likewise to be considered advantageous that compounds of the formula (I) can be used in particular also for transgenic seed. Furthermore, compounds of the formula (I) can be employed in combination with compositions or compounds of signalling technology, leading to better colonization by symbionts such as, for example, rhizobia, mycorrhizae and/or endophytic bacteria or fungi, and/or to optimized nitrogen fixation. The compounds of the formula (I) are suitable for protection of seed of any plant variety which is used in agriculture, in the greenhouse, in forests or in horticulture. In particular, this takes the form of seed of cereals (for example wheat, barley, rye, millet and oats), corn, cotton, soya beans, rice, potatoes, sunflowers, coffee, tobacco, canola, oilseed rape, beets (for example sugarbeets and fodder beets), peanuts, vegetables (for example tomatoes, cucumbers, bean, cruciferous vegetables, onions and lettuce), fruit plants, lawns and ornamental plants. The treatment of the seed of cereals (such as wheat, barley, rye and oats), maize, soya beans, cotton, canola, oilseed rape, vegetables and rice is of particular importance. As already mentioned above, the treatment of transgenic seed with a compound of the formula (I) is also of particular importance. This takes the form of seed of plants which, as a rule, comprise at least one heterologous gene which governs the expression of a polypeptide with in particular insecticidal and/or nematicidal properties. The heterologous genes in transgenic seed can originate from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. The present invention is particularly suitable for the treatment of transgenic seed which comprises at least one heterologous gene originating from Bacillus sp. It is particularly preferably a heterologous gene derived from Bacillus thuringiensis. In the context of the present invention, the compound of the formula (I) is applied to the seed. Preferably, the seed is treated in a state in which it is stable enough to avoid damage during treatment. In general, the seed may be treated at any point in time between harvest and sowing. The seed usually used has been separated from the plant and freed from cobs, shells, stalks, coats, hairs or the flesh of the fruits. For example, it is possible to use seed which has been harvested, cleaned and dried down to a moisture content which allows storage. Alternatively, it is also possible to use seed which, after drying, has been treated with, for example, water and then dried again, for example priming. In the case of rice seed, it is also possible to use seed which has been soaked, for example in water to a certain stage of the rice embryo (‘pigeon breast stage’), stimulating the germination and a more uniform emergence. When treating the seed, care must generally be taken that the amount of the compound of the formula (I) applied to the seed and/or the amount of further additives is chosen in such a way that the germination of the seed is not adversely affected, or that the resulting plant is not damaged. This must be ensured particularly in the case of active compounds which can exhibit phytotoxic effects at certain application rates. In general, the compounds of the formula (I) are applied to the seed in a suitable formulation. Suitable formulations and processes for seed treatment are known to the person skilled in the art. The compounds of the formula (I) can be converted to the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other coating compositions for seed, and also ULV formulations. These formulations are prepared in a known manner, by mixing the compounds of the formula (I) with customary additives such as, for example, customary extenders and also solvents or diluents, colorants, wetting agents, dispersants, emulsifiers, antifoams, preservatives, secondary thickeners, adhesives, gibberellins and also water. Colorants which may be present in the seed-dressing formulations which can be used in accordance with the invention are all colorants which are customary for such purposes. It is possible to use either pigments, which are sparingly soluble in water, or dyes, which are soluble in water. Examples include the dyes known by the names Rhodamine B, C.I. Pigment Red 112 and C.I. Solvent Red 1. Useful wetting agents which may be present in the seed dressing formulations usable in accordance with the invention are all substances which promote wetting and which are conventionally used for the formulation of agrochemically active compounds. Preference is given to using alkylnaphthalenesulphonates, such as diisopropyl- or diisobutylnaphthalenesulphonates. Useful dispersants and/or emulsifiers which may be present in the seed dressing formulations usable in accordance with the invention are all nonionic, anionic and cationic dispersants conventionally used for the formulation of active agrochemical ingredients. Preference is given to using nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants. Suitable nonionic dispersants include in particular ethylene oxide/propylene oxide block polymers, alkylphenol polyglycol ethers and tristryrylphenol polyglycol ethers, and the phosphated or sulphated derivatives thereof. Suitable anionic dispersants are in particular lignosulphonates, polyacrylic acid salts and arylsulphonate/formaldehyde condensates. Antifoams which may be present in the seed dressing formulations usable in accordance with the invention are all foam-inhibiting substances conventionally used for the formulation of active agrochemical ingredients. Preference is given to using silicone antifoams and magnesium stearate. Preservatives which may be present in the seed dressing formulations usable in accordance with the invention are all substances usable for such purposes in agrochemical compositions. Examples include dichlorophene and benzyl alcohol hemiformal. Secondary thickeners which may be present in the seed dressing formulations usable in accordance with the invention are all substances which can be used for such purposes in agrochemical compositions. Cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica are preferred. Adhesives which may be present in the seed dressing formulations usable in accordance with the invention are all customary binders usable in seed dressing products. Polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose may be mentioned as being preferred. Gibberellins which can be present in the seed-dressing formulations which can be used in accordance with the invention are preferably the gibberellins A1, A3 (= gibberellic acid), A4 and A7; gibberellic acid is especially preferably used. The gibberellins are known (cf. R. Wegler "Chemie der Pflanzenschutz- and Schädlingsbekämpfungsmittel", vol.2, Springer Verlag, 1970, pp.401-412). The seed dressing formulations usable in accordance with the invention can be used to treat a wide variety of different kinds of seed either directly or after prior dilution with water. For instance, the concentrates or the preparations obtainable therefrom by dilution with water can be used to dress the seed of cereals, such as wheat, barley, rye, oats, and triticale, and also the seed of maize, rice, oilseed rape, peas, beans, cotton, sunflowers, soya beans and beets, or else a wide variety of different vegetable seed. The seed dressing formulations usable in accordance with the invention, or the dilute use forms thereof, can also be used to dress seed of transgenic plants. For treatment of seed with the seed dressing formulations usable in accordance with the invention, or the use forms prepared therefrom by adding water, all mixing units usable customarily for the seed dressing are useful. Specifically, the procedure in the seed dressing is to place the seed into a mixer, operated batch- wise or continously, to add the particular desired amount of seed dressing formulations, either as such or after prior dilution with water, and to mix everything until the formulation is distributed homogeneously on the seed. If appropriate, this is followed by a drying operation. The application rate of the seed dressing formulations usable in accordance with the invention can be varied within a relatively wide range. It is guided by the particular content of the compounds of the formula (I) in the formulations and by the seed. The application rates of the compound of the formula (I) are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed. Animal health In the animal health field, i.e. in the field of veterinary medicine, the compounds of the formula (I) are active against animal parasites, in particular ectoparasites or endoparasites. Ectoparasites are typically and preferably arthropods, in particular insects or acarids. In the field of veterinary medicine the compounds of the formula (I) are suitable, with favourable toxicity in warm blooded animals, for controlling parasites which occur in animal breeding and animal husbandry in livestock, breeding, zoo, laboratory, experimental and domestic animals (companion animals). They are active against all or specific stages of development of the parasites. Agricultural livestock (farm animals) include, for example, mammals, such as, sheep, goats, horses, donkeys, camels, buffaloes, rabbits, reindeers, fallow deers, and in particular cattle and pigs; or poultry, such as turkeys, ducks, geese, and in particular chickens; or fish or crustaceans, e.g. in aquaculture; or, as the case may be, insects such as bees. Domestic animals or companion animals include, for example, mammals, such as hamsters, guinea pigs, rats, mice, chinchillas, ferrets or in particular dogs, cats; cage birds; reptiles; amphibians or aquarium fish. According to a particular embodiment, the compounds of the formula (I) are administered to mammals. According to another particular embodiment, the compounds of the formula (I) are administered to birds, namely cage birds or in particular poultry. According to another particular embodiment, the compounds of the formula (I) are administered to farm animals or companion animals, in particular to companion animals such as cats and dogs. By using the compounds of the formula (I) to control animal parasites, it is intended to reduce or prevent illness, cases of deaths and performance reductions (in the case of meat, milk, wool, hides, eggs, honey and the like), so that more economical and simpler animal keeping is made possible and better animal well-being is achievable. The term “control” or "controlling", as used herein with regard to the animal health field, means that the compounds of the formula (I) are effective in reducing the incidence of the respective parasite in an animal infected with such parasites to innocuous levels. More specifically, "controlling", as used herein, means that the compounds of the formula (I) are effective in killing the respective parasite, inhibiting its growth, or inhibiting its proliferation. Exemplary arthropods include, without any limitation from the order of the Anoplurida, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.; from the order of the Mallophagida and the suborders Amblycerina and Ischnocerina, for example Bovicola spp., Damalina spp., Felicola spp., Lepikentron spp., Menopon spp., Trichodectes spp., Trimenopon spp., Trinoton spp., Werneckiella spp.; from the order of the Diptera and the suborders Nematocerina and Brachycerina, for example Aedes spp., Anopheles spp., Atylotus spp., Braula spp., Calliphora spp., Chrysomyia spp., Chrysops spp., Culex spp., Culicoides spp., Eusimulium spp., Fannia spp., Gasterophilus spp., Glossina spp., Haematobia spp., Haematopota spp., Hippobosca spp., Hybomitra spp., Hydrotaea spp., Hypoderma spp., Lipoptena spp., Lucilia spp., Lutzomyia spp., Melophagus spp., Morellia spp., Musca spp., Odagmia spp., Oestrus spp., Philipomyia spp., Phlebotomus spp., Rhinoestrus spp., Sarcophaga spp., Simulium spp., Stomoxys spp., Tabanus spp., Tipula spp., Wilhelmia spp., Wohlfahrtia spp. from the order of the Siphonapterida, for example Ceratophyllus spp.; Ctenocephalides spp., Pulex spp., Tunga spp., Xenopsylla spp.; from the order of the Heteropterida, for example Cimex spp., Panstrongylus spp., Rhodnius spp., Triatoma spp.; as well as nuisance and hygiene pests from the order of the Blattarida. Further, among the arthropods, the following acari may be mentioned by way of example, without any limitation: from the subclass of the Acari (Acarina) and the order of the Metastigmata, for example, from the family of argasidae like Argas spp., Ornithodorus spp., Otobius spp., from the family of Ixodidae like Amblyomma spp., Dermacentor spp., Haemaphysalis spp., Hyalomma spp., Ixodes spp., Rhipicephalus (Boophilus) spp , Rhipicephalus spp. (the original genus of multi host ticks); from the order of mesostigmata like Dermanyssus spp., Ornithonyssus spp., Pneumonyssus spp., Raillietia spp., Sternostoma spp., Tropilaelaps spp., Varroa spp.; from the order of the Actinedida (Prostigmata), for example Acarapis spp., Cheyletiella spp., Demodex spp., Listrophorus spp., Myobia spp., Neotrombicula spp., Ornithocheyletia spp., Psorergates spp., Trombicula spp.; and from the order of the Acaridida (Astigmata), for example Acarus spp., Caloglyphus spp., Chorioptes spp., Cytodites spp., Hypodectes spp., Knemidocoptes spp., Laminosioptes spp., Notoedres spp., Otodectes spp., Psoroptes spp., Pterolichus spp., Sarcoptes spp., Trixacarus spp., Tyrophagus spp. In a particular aspect the compounds of the formula (I) are effective in reducing the incidence of parasites selected from arthropods, more particularly from the subclass of the Acari and insects, in an animal infected with such parasites to innocuous levels. In the veterinary field and in animal keeping, the administration of the compounds of the formula (I) is carried out by methods generally known in the art, such as enterally, parenterally, dermally or nasally, in the form of suitable preparations. Administration can be carried out prophylactically, methaphylactically or therapeutically. Thus, one embodiment of the present invention refers to the compounds of the formula (I) for use as a medicament. Another aspect refers to the compounds of the formula (I) for use as an antiendoparasitical agent. Another aspect refers to the compounds of the formula (I) for use as an antiectoparasitical agent, in particular an arthropodicidal agent, more particular an insecticidal agent or acaricidal agent. Further aspects of the invention are veterinary formulations, comprising an effective amount of at least one compound of the formula (I) and at least one of the following: pharmaceutically acceptable excipient (e.g. solid or liquid diluents), pharmaceutically acceptable auxiliary (e.g. surfactants), in particular a pharmaceutically acceptable excipient and/or pharmaceutically acceptable auxiliary which is normally used in veterinary formulations. A related aspect of the invention is a method for preparing a veterinary formulation as described herein, comprising the step of mixing at least one compound of the formula (I) with pharmaceutically acceptable excipients and/or auxiliaries , in particular with pharmaceutically acceptable excipients and/or auxiliaries which are normally used in veterinary formulations. Another particular aspect of the invention are veterinary formulations, selected from the group of ectoparasiticidal and endoparasiticidal formulations, more particular an arthropodicidal formulations, even more particular selected from the group of nematicidal, platyhelminthicidal, acanthocephalicidal, pentastomicidal, insecticidal, and acaricidal formulations, in accordance with the mentioned aspects, as well as their methods for preparation. Another aspect refers to a method for treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, by applying an effective amount of a compound of the formula (I) to an animal, in particular a non-human animal, in need thereof. Another aspect refers to a method for treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, by applying a veterinary formulation as defined herein to an animal, in particular a non-human animal, in need thereof. Another aspect refers to the use of the compounds of the formula (I) in the treatment of a parasitic infection, in particular an infection by a parasite selected from the group of ectoparasites and endoparasites mentioned herein, in an animal, in particular a non-human animal. In the present context of the animal health or veterinary field, the term "treatment" includes prophylactic, metaphylactic or therapeutical treatment. In a particular embodiment, mixtures of at least one compound of the formula (I) with other active ingredients, particularly with endo- and ectoparasiticides, for the veterinary field are provided herewith. In the field of animal health “mixture” not only means that two (or more) different active ingredients are formulated in a joint formulation and are accordingly applied together but also refers to products which comprise separate formulations for each active compound. Accordingly, if more than two active compounds are to be applied, all active compounds may be formulated in a joint formulation or all active compounds may be formulated in separate formulations; also feasible are mixed forms where some of the active compounds are formulated jointly and some of the active compounds are formulated separately. Separate formulations allow the separate or successive application of the active compounds in question. The active compounds specified herein by their common names are known and described, for example, in the Pesticide Manual (see above) or can be searched in the internet (e.g. http://www.alanwood.net/pesticides). Exemplary active ingredients from the group of ectoparasiticides, as mixing partners, include, without limitation insecticides and acaricides listed in detail above. Further active ingredients which may be used are listed below following the aforementioned classification which is based on the current IRAC Mode of Action Classification Scheme: (1) Acetylcholinesterase (AChE) inhibitors; (2) GABA-gated chloride channel blockers; (3) Sodium channel modulators; (4) Nicotinic acetylcholine receptor (nAChR) competitive modulators; (5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators; (6) Glutamate-gated chloride channel (GluCl) allosteric modulators; (7) Juvenile hormone mimics; (8) Miscellaneous non-specific (multi-site) inhibitors; (9) Modulators of Chordotonal Organs; (10) Mite growth inhibitors; (12) Inhibitors of mitochondrial ATP synthase, such as, ATP disruptors; (13) Uncouplers of oxidative phosphorylation via disruption of the proton gradient; (14) Nicotinic acetylcholine receptor channel blockers; (15) Inhibitors of chitin biosynthesis, type 0; (16) Inhibitors of chitin biosynthesis, type 1; (17) Moulting disruptor (in particular for Diptera, i.e. dipterans); (18) Ecdysone receptor agonists; (19) Octopamine receptor agonists; (21) Mitochondrial complex I electron transport inhibitors; (25) Mitochondrial complex II electron transport inhibitors; (20) Mitochondrial complex III electron transport inhibitors; (22) Voltage-dependent sodium channel blockers; (23) Inhibitors of acetyl CoA carboxylase; (28) Ryanodine receptor modulators; Active compounds with unknown or non-specific mode of action, e.g., fentrifanil, fenoxacrim, cycloprene, chlorobenzilate, chlordimeform, flubenzimine, dicyclanil, amidoflumet, quinomethionate, triarathene, clothiazoben, tetrasul, potassium oleate, petroleum, metoxadiazone, gossyplure, flutenzin, bromopropylate, cryolite; Compounds from other classes, e.g. butacarb, dimetilan, cloethocarb, phosphocarb, pirimiphos (-ethyl), parathion (-ethyl), methacrifos, isopropyl o-salicylate, trichlorfon, tigolaner, sulprofos, propaphos, sebufos, pyridathion, prothoate, dichlofenthion, demeton-S-methylsulphone, isazofos, cyanofenphos, dialifos, carbophenothion, autathiofos, aromfenvinfos (-methyl), azinphos (-ethyl), chlorpyrifos (-ethyl), fosmethilan, iodofenphos, dioxabenzofos, formothion, fonofos, flupyrazofos, fensulfothion, etrimfos; organochlorines, e.g. camphechlor, lindane, heptachlor; or phenylpyrazoles, e.g. acetoprole, pyrafluprole, pyriprole, vaniliprole, sisapronil; or isoxazolines, e.g. sarolaner, afoxolaner, lotilaner, fluralaner; pyrethroids, e.g. (cis-, trans-), metofluthrin, profluthrin, flufenprox, flubrocythrinate, fubfenprox, fenfluthrin, protrifenbute, pyresmethrin, RU15525, terallethrin, cis-resmethrin, heptafluthrin, , bioethanomethrin, biopermethrin, fenpyrithrin, cis-cypermethrin, cis-permethrin, clocythrin, cyhalothrin (lambda-), chlovaporthrin, or halogenated carbonhydrogen compounds (HCHs), neonicotinoids, e.g. nithiazine dicloromezotiaz, triflumezopyrim macrocyclic lactones, e.g. nemadectin, ivermectin, latidectin, moxidectin, selamectin, eprinomectin, doramectin, emamectin benzoate; milbemycin oxime triprene, epofenonane, diofenolan; Biologicals, hormones or pheromones, for example natural products, e.g. thuringiensin, codlemone or neem components dinitrophenols, e.g. dinocap, dinobuton, binapacryl; benzoylureas, e.g. fluazuron, penfluron, amidine derivatives, e.g. chlormebuform, cymiazole, demiditraz Bee hive varroa acaricides, for example organic acids, e.g. formic acid, oxalic acid. Exemplary active ingredients from the group of endoparasiticides, as mixing partners, include, without limitation, anthelmintically active compounds and antiprotozoal active compounds. Anthelmintically active compounds, including, without limitation, the following nematicidally, trematicidally and/or cestocidally active compounds: from the class of macrocyclic lactones, for example: eprinomectin, abamectin, nemadectin, moxidectin, doramectin, selamectin, lepimectin, latidectin, milbemectin, ivermectin, emamectin, milbemycin; from the class of benzimidazoles and probenzimidazoles, for example: oxibendazole, mebendazole, triclabendazole, thiophanate, parbendazole, oxfendazole, netobimin, fenbendazole, febantel, thiabendazole, cyclobendazole, cambendazole, albendazole-sulphoxide, albendazole, flubendazole; from the class of depsipeptides, preferably cyclic depsipetides, in particular 24-membered cyclic depsipeptides, for example: emodepside, PF1022A; from the class of tetrahydropyrimidines, for example: morantel, pyrantel, oxantel; from the class of imidazothiazoles, for example: butamisole, levamisole, tetramisole; from the class of aminophenylamidines, for example: amidantel, deacylated amidantel (dAMD), tribendimidine; from the class of aminoacetonitriles, for example: monepantel; from the class of paraherquamides, for example: paraherquamide, derquantel; from the class of salicylanilides, for example: tribromsalan, bromoxanide, brotianide, clioxanide, closantel, niclosamide, oxyclozanide, rafoxanide; from the class of substituted phenols, for example: nitroxynil, bithionol, disophenol, hexachlorophene, niclofolan, meniclopholan; from the class of organophosphates, for example: trichlorfon, naphthalofos, dichlorvos/DDVP, crufomate, coumaphos, haloxon; from the class of piperazinones / quinolines, for example: praziquantel, epsiprantel; from the class of piperazines, for example: piperazine, hydroxyzine; from the class of tetracyclines, for example: tetracyclin, chlorotetracycline, doxycyclin, oxytetracyclin, rolitetracyclin; from diverse other classes, for example: bunamidine, niridazole, resorantel, omphalotin, oltipraz, nitroscanate, nitroxynile, oxamniquine, mirasan, miracil, lucanthone, hycanthone, hetolin, emetine, diethylcarbamazine, dichlorophen, diamfenetide, clonazepam, bephenium, amoscanate, clorsulon. Antiprotozoal active compounds, including, without limitation, the following active compounds: from the class of triazines, for example: diclazuril, ponazuril, letrazuril, toltrazuril; from the class of polylether ionophore, for example: monensin, salinomycin, maduramicin, narasin; from the class of macrocyclic lactones, for example: milbemycin, erythromycin; from the class of quinolones, for example: enrofloxacin, pradofloxacin; from the class of quinines, for example: chloroquine; from the class of pyrimidines, for example: pyrimethamine; from the class of sulfonamides, for example: sulfaquinoxaline, trimethoprim, sulfaclozin; from the class of thiamines, for example: amprolium; from the class of lincosamides, for example: clindamycin; from the class of carbanilides, for example: imidocarb; from the class of nitrofuranes, for example: nifurtimox; from the class of quinazolinone alkaloids, for example: halofuginon; from diverse other classes, for example: oxamniquin, paromomycin; from the class of vaccines or antigenes from microorganisms, for example: Babesia canis rossi, Eimeria tenella, Eimeria praecox, Eimeria necatrix, Eimeria mitis, Eimeria maxima, Eimeria brunetti, Eimeria acervulina, Babesia canis vogeli, Leishmania infantum, Babesia canis canis, Dictyocaulus viviparus. All named mixing partners can, if their functional groups enable this, optionally form salts with suitable bases or acids. Vector control The compounds of the formula (I) can also be used in vector control. For the purpose of the present invention, a vector is an arthropod, in particular an insect or arachnid, capable of transmitting pathogens such as, for example, viruses, worms, single-cell organisms and bacteria from a reservoir (plant, animal, human, etc.) to a host. The pathogens can be transmitted either mechanically (for example trachoma by non-stinging flies) to a host, or by injection (for example malaria parasites by mosquitoes) into a host. Examples of vectors and the diseases or pathogens they transmit are: 1) Mosquitoes - Anopheles: malaria, filariasis; - Culex: Japanese encephalitis, other viral diseases, filariasis, transmission of other worms; - Aedes: yellow fever, dengue fever, other viral diseases, filariasis; - Simuliidae: transmission of worms, in particular Onchocerca volvulus; - Psychodidae: transmission of leishmaniasis 2) Lice: skin infections, epidemic typhus; 3) Fleas: plague, endemic typhus, cestodes; 4) Flies: sleeping sickness (trypanosomiasis); cholera, other bacterial diseases; 5) Mites: acariosis, epidemic typhus, rickettsialpox, tularaemia, Saint Louis encephalitis, tick-borne encephalitis (TBE), Crimean–Congo haemorrhagic fever, borreliosis; 6) Ticks: borellioses such as Borrelia burgdorferi sensu lato., Borrelia duttoni, tick-borne encephalitis, Q fever (Coxiella burnetii), babesioses (Babesia canis canis), ehrlichiosis. Examples of vectors in the sense of the present invention are insects, for example aphids, flies, leafhoppers or thrips, which are capable of transmitting plant viruses to plants. Other vectors capable of transmitting plant viruses are spider mites, lice, beetles and nematodes. Further examples of vectors in the sense of the present invention are insects and arachnids such as mosquitoes, in particular of the genera Aedes, Anopheles, for example A. gambiae, A. arabiensis, A. funestus, A. dirus (malaria) and Culex, psychodids such as Phlebotomus, Lutzomyia, lice, fleas, flies, mites and ticks capable of transmitting pathogens to animals and/or humans. Vector control is also possible if the compounds of the formula (I) are resistance-breaking. Compounds of the formula (I) are suitable for use in the prevention of diseases and/or pathogens transmitted by vectors. Thus, a further aspect of the present invention is the use of compounds of the formula (I) for vector control, for example in agriculture, in horticulture, in gardens and in leisure facilities, and also in the protection of materials and stored products. Protection of industrial materials The compounds of the formula (I) are suitable for protecting industrial materials against attack or destruction by insects, for example from the orders Coleoptera, Hymenoptera, Isoptera, Lepidoptera, Psocoptera and Zygentoma. Industrial materials in the present context are understood to mean inanimate materials, such as preferably plastics, adhesives, sizes, papers and cards, leather, wood, processed wood products and coating compositions. The use of the invention for protecting wood is particularly preferred. In a further embodiment, the compounds of the formula (I) are used together with at least one further insecticide and/or at least one fungicide. In a further embodiment, the compounds of the formula (I) are present as a ready-to-use pesticide, i.e. they can be applied to the material in question without further modifications. Suitable further insecticides or fungicides are in particular those mentioned above. Surprisingly, it has also been found that the compounds of the formula (I) can be employed for protecting objects which come into contact with saltwater or brackish water, in particular hulls, screens, nets, buildings, moorings and signalling systems, against fouling. Likewise, the compounds of the formula (I), alone or in combinations with other active compounds, can be used as antifouling agents. Control of animal pests in the hygiene sector The compounds of the formula (I) are suitable for controlling animal pests in the hygiene sector. In particular, the invention can be applied in the domestic sector, in the hygiene sector and in the protection of stored products, especially for controlling insects, arachnids, ticks and mites encountered in enclosed spaces such as dwellings, factory halls, offices, vehicle cabins, animal husbandries. For controlling animal pests, the compounds of the formula (I) are used alone or in combination with other active compounds and/or auxiliaries. They are preferably used in domestic insecticide products. The compounds of the formula (I) are effective against sensitive and resistant species, and against all developmental stages. These pests include, for example, pests from the class Arachnida, from the orders Scorpiones, Araneae and Opiliones, from the classes Chilopoda and Diplopoda, from the class Insecta the order Blattodea, from the orders Coleoptera, Dermaptera, Diptera, Heteroptera, Hymenoptera, Isoptera, Lepidoptera, Phthiraptera, Psocoptera, Saltatoria or Orthoptera, Siphonaptera and Zygentoma and from the class Malacostraca the order Isopoda. They are used, for example, in aerosols, pressure-free spray products, for example pump and atomizer sprays, automatic fogging systems, foggers, foams, gels, evaporator products with evaporator tablets made of cellulose or plastic, liquid evaporators, gel and membrane evaporators, propeller-driven evaporators, energy-free, or passive, evaporation systems, moth papers, moth bags and moth gels, as granules or dusts, in baits for spreading or in bait stations. Abbreviations and Symbols AcOH: acetic acid aq.: aqueous BINAP 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl br.: broad d: doublet dppf 1,1'-Bis(diphenylphosphino)ferrocene DCC: N,N’-dicyclohexylcarbodiimide DCM dichloromethane DIPEA: diisopropylethylamine DIAD Diisopropylazodicarboxylate DMF: N,N-dimethylformamide DMSO: dimethylsulfoxide ee: enantiomeric excess eq.: equivalent ES: electrospray ionization EtOAc: ethyl acetate HATU: 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxid hexafluorophosphate HOBt: 1-hydroxybenzotriazole hydrate HPLC: high performance liquid chromatography iPrOH: isopropanol J: coupling constant LCMS: liquid chromatography-mass spectrometry m/z: mass-to-charge ratio M: molarity m: multiplet MeCN acetonitrile MeOH: methanol MTBE tert-butyl methyl ether NMR: nuclear magnetic resonance q: quartet r. t.: room temperature Rt: retention time s: singlet sat.: saturated T: temperature TMP 2,2,6,6-tetramethylpiperidine t: triplet T3P®: propylphosphonic anhydride THF: tetrahydrofuran wt.: weight XantPHOS 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene (CAS RN 161265-03-8) δ: chemical shift λ: wavelength Description of the processes and intermediates Compounds of formula (I) may be prepared as illustrated in the following scheme 1 where R1, R2, R3,R4, R5, R6 are as previously defined. Scheme 1
Figure imgf000101_0001
The synthesis starts with a pyrazine of formula (II) which carries residues R5 and R6, as well as one group X1 which can be chlorine, bromine or iodine. These compounds are commercially available or can be made according to methods described in the art. In a first transformation, the hydrogen atom next to X1 is abstracted and replaced by a metal fragment consisting of a main group metal such as Li, Mg, Zn and appropriate ligands L. An example for such a transformation is given by F. Buron, N. Pié, A. Turck, G, Quéguigner, J. Org. Chem.2005, 70, 2616-2621, showing the lithiation of 2-chloropyrazine with Li-TMP (2,2,6,6-tetramethylpiperidyl-lithium base) in THF. Other TMP based reagents are summarized in a review by T. Klatt, J.T. Markiewicz, C. Sämann, P. Knochel, J. Org. Chem. 2014, 79, 4253-4269. The metalated intermediate (III) is then trapped in situ with an aldehyde (IV) to give the secondary alcohol (V). Metalation and reaction with the aldehyde are typically carried out in one pot in a polar, nonprotic solvent such as THF, diethyl ether, dioxane. The temperature in the metalation step is typically below 0 °C, preferably at -78 °C in a dry ice bath. After the addition of the aldehyde, the temperature may be raised to 0 °C or even room temperature. Instead of the one-pot procedure, the organometal intermediate may also be prepared in advance and then be added to a solution of the aldehyde in a suitable nonprotic solvent such as, for instance, THF, ether or toluene. The subsequent step consists in the replacement of the hydroxy group from intermediate (V) by a fully protected nitrogen resulting in intermediates of formula (VII). PG1 and PG2 may be either two independent protecting groups or may be joined to form one cyclic protecting group. Depending on the respective reaction and the protecting group used the other of PG1 and PG2 may also represent hydrogen. Examples for protecting groups suitable for the protection of amino functionalities can be found in T.W. Greene, P.G.M. Wuts “Protective Groups in Organic Chemistry” 3rd edition, Wiley Interscience, New York 1999, e.g. the Boc-group. Preferentially, the phthalimide protecting group is used. The replacement of the hydroxy group may be carried out either by converting the alcohol into a halogenide by a method known in the art, e.g. Appel reaction, treatment with sulfuryl chloride etc and subsequent nucleophilic substitution by phthalimide, or, preferably, by direct conversion of intermediate (V) with phthalimide in a Mitsunobu reaction with DIAD and triphenylphosphine a in a suitable solvent such as THF at temperature ranging from -40 °C to 100 °C, preferentially from 0 °C to room temperature. Introduction of R4 occurs in the next step using a cross coupling reaction with reagent (VIII) which carries the leaving group X2. X2 may be a trialkyl stannyl residue, a boronic acid, a boronic ester or a metal fragment M(Ln) with a metal such as Ni, Zn, Mg and appropriate ligands L. The cross coupling reaction is typically catalyzed by a transition metal catalyst such as a palladium or copper catalyst with appropriate ligands. A broad survey on cross coupling reactions is available in F. Diederich, A. de Meijere, “Metal catalyzed Cross Coupling Reactions, Second Edition”, Wiley Online Library, online ISBN: 9783527619535. A variation of the cross coupling reaction could be to replace the moiety X1 from intermediate (VII) by a trialkyl trialkyl stannyl residue, a boronic acid, a boronic ester or a metal fragment M(Ln) with a metal such as Ni, Zn, Mg and appropriate ligands L. In this case, intermediate (VIII) would have to carry a group X2 chosen from, for instance, Cl, Br, I, triflate or similar. Suitable conditions for a coupling of X1 = Cl, Br or I and X2 = trialkyl stannyl, boronic acid or boronic ester may involve the use of 0.01-0.5 equivalents of a palladium source such as PdCl2(dppf) x DCM, palldium diacetate, tetrakistriphenylphosphine palladium or other compounds together with a ligand. Ligands can be chosen from phosphine ligands or N-heterocyclic carbene ligands, an overview of some ligands is given in R. Martin, S.L. Buchwald, Acc. Chem. Res.2008, 61, 1461-1473. The product (IX) of the cross coupling reaction has to be deprotected in the next step. In case a phthalimide protecting group is used, this can be achieved by reacting (IX) with hydrazine hydrate in an appropriate solvent such as ethanol at room temperature or above room temperature. Compounds of formula (I) can be obtained by reacting intermediates (X) with carboxylic acid derivatives (XI) wherein X3 is Cl, O-acyl or OH. In cases where X is Cl or O-acyl, (X) and (XI) are directly reacted in the presence of a base such as, for instance, DIPEA, triethylamine or N-methylmorpholine in a solvent such as DMF, THF or similar. In cases where X is OH, the acid (XI) needs to be activated using a coupling agent such as HATU, TBTU, TCTU, PyBOP etc or, alternatively, converting it into the corresponding acid chloride or an anhydride prior to react it with (X) as described above. The resulting products (Ia) are compounds of the invention where R1 is H. In order to achieve compounds with R1 other than hydrogen, an alkylation reaction with alkylating agent (XII) may be used. Examples of leaving groups LG are Cl, Br, I, tosylate, mesylate or triflate groups. The reaction may be carried out by mixing the reagents (Ia) and (XII) together with a base, such as K2CO3 or DIPEA in a suitable solvent, such as acetonitrile or DMF and letting them react at a temperature in the range 20 to 100 °C. Compounds of formula (Ib) may then be isolated and, if necessary and desired, purified using techniques well known in the art, such as chromatography. If in the compounds (I) R4 is a pyridine-group, then it is preferred that in the Scheme 1 supra X1 is Cl, X2 is Zn-Cl, the Pd-catalyst is a Pd2(dba)3 catalyst and the ligand L is X-Phos. If in the compounds (I) R4 is a pyrimidine-group, then it is preferred that in the Scheme 1 supra X1 is Cl, X2 is SnBu3, the Pd-catalyst is a PdCl2*2APhos catalyst and ZnCl2 is added as an additive. If in the compounds (I) R4 is a thiazole-group, then it is preferred that in the Scheme 1 supra X1 is Cl, X2 is SnBu3, the Pd-catalyst is a PdCl2*2PPh3 catalyst and the ligand L is PPh3.
Figure imgf000104_0001
In a variant of the above described synthetic pathway, the Mitsunobu reaction and the cross coupling reaction may be applied in inverse order as displayed in Scheme 2. In this case, the introduction of R4 by one of the cross coupling methods described above results in intermediate XIII which is then further converted into intermediate IX by a Mitsunobu reaction as described above. In certain cases, this may give an advantage in terms of yield or practicability. Regarding the meaning of the group PG1 and PG2 reference is made to the definition supra. In cases where R4 is bound to the pyrazine moiety by a nitrogen atom, X1 of intermediates V and VII is preferentially halogen (in particular Cl, Br or I), and X2 is hydrogen bound to a nitrogen atom within R4. Specifically, this applies to cases where R4 is optionally substituted pyrazole or imidazole. The general strategy for these molecules may follow the order of steps displayed in either Scheme 1 or Scheme 2. Preferentially, the introduction of a pyrazole or imidazole is carried out prior to the introduction of the amine as shown in Scheme 2. The actual cross coupling step is carried out using a metal catalyst, optionally ligands, a base and a solvent. Metal catalysts useful in this step comprise copper(I) and copper(II) salts, preferentially copper(I) halides such as, for instance, copper(I) iodide. The use of a ligand may be beneficial, the choice of a suitable ligand depends on the metal catalyst. In the case of copper(I) salts, 1,2- diamines such as TMEDA or trans-N,N,N',N'-tetramethylcyclohexane-1,2-diamine are used. A catalytic amount of the metal catalyst and the ligand is used, typically in the range of 0.01-0.5 molar equivalents of each of them. As a base, alkali or earth alkali carbonates may be used such as, for instance, calcium carbonate, sodium carbonate, potassium carbonate or cesium carbonate. Solvents include DMF, THF, 1,4- dioxane toluene, chlorobenzene or other organic solvents usually employed for cross coupling reactions. The reaction is performed at room temperature or above, preferrably at 100-120 °C. If R4 is a pyrazole, the preferred conditions for cross coupling comprise using 0.3 equiovalents of copper(I) iodide, 0.3 eqivalents of trans-N,N,N',N'-tetramethylcyclohexane-1,2-diamine, an excess of potassium carbonate in toluene under reflux. In certain cases, compounds of the invention are accessible via modifications of the substituents in the aftermath of the introduction of R4. These operations can be carried out either in the presence of the R2 moiety or, as an alternative, prior to the introduction of R2 using a suitably protected intermediate according to formula IX (see Scheme I). For instance, an ester group placed on R4 may be saponified by standard methodology. Preferred methods for the saponification of esters comprise lithium hydroxide or sodium hydroxide in a mixture of solvents such as methanol and THF with water at a temperature ranging from room temperature to reflux, or lithium iodide in pyridine at a temperature above 100 °C. The resulting carboxylic acid can be converted into carboxamides by the use of coupling agents such as TBTU, HATU, EDCI or other reagents known in the art. Carboxylic esters can also be converted into cyanides using Burgess reagent. Alternatively, carboxylic acids can be converted into amines using a Curtius rearrangement, and the resulting amino group can then be acylated to give a carboxamide linked to R4 via a nitrogen atom by the use of coupling agents such as TBTU, HATU, EDCI or other reagents known in the art. The processes according to the invention for the preparation of compounds of the formula (I) are preferably performed using a diluent. Useful diluents for performance of the processes according to the invention are, as well as water, all inert solvents. Examples include: halohydrocarbons (for example chlorohydrocarbons such as tetrachloroethylene, tetrachloroethane, dichloropropane, methylene chloride, dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichloroethylene, pentachloroethane, difluorobenzene, 1,2-dichloroethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene), alcohols (for example methanol, ethanol, isopropanol, butanol), ethers (for example ethyl propyl ether, methyl tert-butyl ether, anisole, phenetole, cyclohexyl methyl ether, dimethyl ether, diethyl ether, dipropyl ether, diisopropyl ether, di-n-butyl ether, diisobutyl ether, diisoamyl ether, ethylene glycol dimethyl ether, tetrahydrofuran, 1,4-dioxane, dichlorodiethyl ether and polyethers of ethylene oxide and/or propylene oxide), amines (for example trimethyl-, triethyl-, tripropyl-, tributylamine, N- methylmorpholine, pyridine and tetramethylenediamine), nitrohydrocarbons (for example nitromethane, nitroethane, nitropropane, nitrobenzene, chloronitrobenzene, o-nitrotoluene); nitriles (for example acetonitrile, propionitrile, butyronitrile, isobutyronitrile, benzonitrile, m-chlorobenzonitrile), tetrahydrothiophene dioxide, dimethyl sulphoxide, tetramethylene sulphoxide, dipropyl sulphoxide, benzyl methyl sulphoxide, diisobutyl sulphoxide, dibutyl sulphoxide, diisoamyl sulphoxide, sulphones (for example dimethyl, diethyl, dipropyl, dibutyl, diphenyl, dihexyl, methyl ethyl, ethyl propyl, ethyl isobutyl and pentamethylene sulphone), aliphatic, cycloaliphatic or aromatic hydrocarbons (for example pentane, hexane, heptane, octane, nonane and technical hydrocarbons), and also what are called "white spirits" with components having boiling points in the range from, for example, 40°C to 250°C, cymene, petroleum fractions within a boiling range from 70°C to 190°C, cyclohexane, methylcyclohexane, petroleum ether, ligroin, benzene, toluene, xylene, esters (for example methyl, ethyl, butyl and isobutyl acetate, dimethyl, dibutyl and ethylene carbonate); amides (for example hexamethylphosphoric triamide, formamide, N-methylformamide, N,N-dimethylformamide, N,N-dipropylformamide, N,N- dibutylformamide, N-methylpyrrolidine, N-methylcaprolactam, 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)- pyrimidine, octylpyrrolidone, octylcaprolactam, 1,3-dimethyl-2-imidazolinedione, N-formylpiperidine, N,N’-diformylpiperazine) and ketones (for example acetone, acetophenone, methyl ethyl ketone, methyl butyl ketone). It is also possible to perform the process according to the invention in mixtures of the solvents and diluents mentioned. When performing the process according to the invention, the reaction temperatures can be varied within a relatively wide range. In general, the temperatures employed are between -30 °C and +150 °C, preferably between -10 °C and +100 °C. The process according to the invention is generally performed under atmospheric pressure. However, it is also possible to perform the process according to the invention under elevated or reduced pressure – generally at absolute pressures between 0.1 bar and 15 bar. To perform the process according to the invention, the starting materials are generally used in approximately equimolar amounts. However, it is also possible to use one of the components in a relatively large excess. The reaction is generally carried out in a suitable diluent in the presence of a reaction auxiliary, optionally also under a protective gas atmosphere (for example under nitrogen, argon or helium) and the reaction mixture is generally stirred at the temperature required for several hours. The workup is performed by customary methods (cf. the preparation examples). The basic reaction auxiliaries used to perform the process according to the invention may be all suitable acid binders. Examples include: alkaline earth metal or alkali metal compounds (e.g. hydroxides, hydrides, oxides and carbonates of lithium, sodium, potassium, magnesium, calcium and barium), amidine bases or guanidine bases (e.g. 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD); diazabicyclo[4.3.0]nonene (DBN), diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]undecene (DBU), cyclohexyltetrabutylguanidine (CyTBG), cyclohexyltetramethylguanidine (CyTMG), N,N,N,N- tetramethyl-1,8-naphthalenediamine, pentamethylpiperidine) and amines, especially tertiary amines (e.g. triethylamine, trimethylamine, tribenzylamine, triisopropylamine, tributylamine, tricyclohexylamine, triamylamine, trihexylamine, N,N-dimethylaniline, N,N-dimethyltoluidine, N,N-dimethyl-p- aminopyridine, N-methylpyrrolidine, N-methylpiperidine, N-methylimidazole, N-methylpyrazole, N- methylmorpholine, N-methylhexamethylenediamine, pyridine, 4-pyrrolidinopyridine, 4- dimethylaminopyridine, quinoline, 2-picoline, 3-picoline, pyrimidine, acridine, N,N,N`,N`- tetramethylenediamine, N,N,N`,N`-tetraethylenediamine, quinoxaline, N-propyldiisopropylamine, N- ethyldiisopropylamine, N,N`-dimethylcyclohexylamine, 2,6-lutidine, 2,4-lutidine or triethylenediamine). The acidic reaction auxiliaries used to perform the process according to the invention include all mineral acids (e.g. hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid or hydriodic acid, and also sulphuric acid, phosphoric acid, phosphorous acid, nitric acid), Lewis acids (e.g. aluminium(III) chloride, boron trifluoride or its etherate, titanium(IV) chloride, tin(IV) chloride) and organic acids (e.g. formic acid, acetic acid, propionic acid, malonic acid, lactic acid, oxalic acid, fumaric acid, adipic acid, stearic acid, tartaric acid, oleic acid, methanesulphonic acid, benzoic acid, benzenesulphonic acid or para-toluenesulphonic acid). The following Examples further illustrate and describe the invention without limiting it. Preparation Examples ANALYTICAL METHODS Method 1 (LC-MS) Instrument: Agilent MS Quad 6150;HPLC: Agilent 1290; column: Waters Acquity UPLC HSS T31.8 µm 50 x 2.1 mm; Eluent A: 1 L water + 0.25 mL 99% formic acid, Eluent B: 1 L acetonitrile + 0.25 mL 99% formic acid; gradient: 0.0 min 90% A → 0.3 min 90% A → 1.7 min 5% A → 3.0 min 5% A oven temp: 50°C; flow: 1.20 mL/min; UV-detection: 205 – 305 nm. Method 2 (LC-MS) Instrument MS: Thermo Scientific FT-MS; instrument for UHPLC+: Thermo Scientific UltiMate 3000; column: Waters, HSST3, 2.1 x 75 mm, C181.8 µm; eluent A: 1 L water + 0.01% formic acid; eluent B: 1 L acetonitrile + 0.01% formic acid; gradient: 0.0 min 10% B → 2.5 min 95% B → 3.5 min 95% B; oven temp:: 50°C; flow: 0.90 mL/min; UV-Detektion: 210 nm/ Optimum Integration Path 210-300 nm Method 3 (LC-MS) Instrument: Waters Single Quad MS System; Instrument Waters UPLC Acquity; column: Waters BEH C181.7 µ 50 x 2.1 mm; Eluent A: 1 L water + 1.0 mL 25% ammonia, Eluent B: 1 L acetonitrile; gradient: 0.0 min 92% A → 0.1 min 92% A → 1.8 min 5% A → 3.5 min 5% A; oven temp.: 50°C; flow: 0.45 mL/min; UV-detection: 210 nm. Method 4 (LC-MS) Analytical Method E Instrument: SHIMADZU LCMS - UFLC 20-AD - LCMS 2020 MS detector; Column: Ascentis Express C182.7 µm, 50 x 3.0 mm; eluent A: water + 0.05 vol % trifluoroacetic acid, eluent B: acetonitrile + 0.05 vol % trifluoroacetic acid; gradient: assigned for each compound; flow 1.2 mL/min; temperature: 40°C; PDA scan: 190 - 400 nm. Method 5 (LC-MS) Analytical Method E1 Instrument: SHIMADZU LCMS - UFLC 20-AD - LCMS 2020 MS detector; Column: Ascentis Express C182.7 µm, 50 x 2.1 mm; eluent A: water + 0.1 vol % formic acid, eluent B: acetonitrile +0.1 vol % formic acid; gradient: assigned for each compound; flow 1.5 mL/min; temperature: 40 °C; PDA scan: 190 - 400 nm. Method 6 (LC-MS) Analytical Method F Instrument: SHIMADZU LCMS - UFLC 20-AD - LCMS 2020 MS detector; Column: Shim-pack XR- ODS, 2.2 µm, 3.0 × 50 mm; eluent A: water + 0.05 vol % trifluoroacetic acid, eluent B: acetonitrile + 0.05 vol % trifluoroacetic acid; gradient: assigned for each compound; flow 1.5 mL/min; temperature: 40°C; PDA scan: 190 - 400 nm. Method 7 (chiral HPLC) Column: Daicel Chiralpak ID, 5 µm 250 x 4.6 mm; Eluent A: iso-hexane, Eluent B: 2-propanol, isocratic at A:B = 1:1, 40°C; flow: 1.0 mL/min; UV-detection: 220 nm. Method 8 (optical rotation) Device: Anton Paar Polarimeter MCP200 Specific rotation [α] (depending wavelength, temperature, optical pathway, solvent and concentration). Method 9 (HPLC-MS) System MS: Waters TOF instrument; System UPLC: Waters Acquity I-CLASS; Column: Waters Acquity UPLC HSS T31.8 µm 50 x 1 mm; Eluent A: 1 l Water + 0.100 ml 99%ige Formic acid, Eluent B: 1 l Acetonitrile + 0.100 ml 99%ige Formic acid; Gradient: 0.0 min 90% A →1.2 min 5% A → 2.0 min 5% A Oven: 50°C; Flow: 0.40 ml/min; UV-Detection: 210 nm. Method 10 (HPLC-MS) System MS: Waters TOF instrument; System UPLC: Waters Acquity I-CLASS; Column: Waters Acquity UPLC HSS T31.8 µm 50 x 1 mm; Eluent A: 1 l Water + 0.100 ml 99%ige Formic acid , Eluent B: 1 l Acetonitrile + 0.100 ml 99%ige Formic acid; Gradient: 0.0 min 95% A → 6.0 min 5% A → 7.5 min 5% A Oven: 50°C; Flow: 0.35 ml/min; UV-Detection: 210 nm. Method 11 (HPLC-MS) Instrument: Waters ACQUITY SQD UPLC System; Column: Waters Acquity UPLC HSS T31.8 µm 50 x 1 mm; Eluent A: 1 l Water + 0.25 ml 99%ige Formic acid , Eluent B: 1 l Acetonitrile + 0.25 ml 99%ige Formic acid; Gradient: 0.0 min 90% A → 1.2 min 5% A → 2.0 min 5% A Oven: 50°C; Flow: 0.40 ml/min; UV-Detection: 210 nm. GENERAL SYNTHETIC METHODS General Synthetic Method 1 Synthesis of MIDA Boronates MIDA boronates were synthesised according to the method described in the literature: G.R. Dick, D.M. Knapp, E.P. Gillis, M.D. Burke, Org. Lett.2010, 12, 2314-2317. On a scale of approximately 100 mmol (calculated on the basis of the 2-bromopyridine derivative), the procedure worked as described here. A 2-bromopyridine derivative (1 equivalent) and tripropan-2-yl borate (1.4 equivalents) were dissolved in THF (200 mL) and this solution was cooled to -78 °C. n- Butyllithium (2.5 M in hexanes, 1.2 equivalents) was slowly added over 90 min. Stirring at -78 °C was maintained for another 60 min, then the cooling bath was removed and the mixture was left to warm to ambient temperature. In a separate 3-neck round bottom flask with a distillation device and an internal thermometer mounted, a solution of 2,2'-(methylimino)diacetic acid (1.6 equivalents) in DMSO (dried over 3 Ǻ molecular sieves, 150 mL) was heated to 125-130 °C. The suspension of the boronate in THF was slowly added over approximately 2 h distilling off the THF and keeping the temperature in a range between 115-125 °C. Eventually, the mixture was stirred another 20 min and then left sitting over night. The DMSO was distilled under vacuum and the residue was adsorbed onto diatomaceous earth and chromatographed over 340 g of silica using a ternary gradient of dichloromethane-ethyl acetate and then etyl acetate-THF. General Synthetic Method 2 Cross-Coupling of MIDA Boronates with halogenated pyrazines (rac)-1-(3-bromopyrazin-2-yl)ethan-1-ol (1 equivalent), a MIDA boronate (1.2 equivalents) and diethanolamine (1.0 equivalents) were dissolved in DMF (ca 4 mL / mmol of halogenated pyrazine) under argon. XPhos Pd G2 (0.1 equivalent), copper(II) acetate (0.5 equivalents) and potassium phosphate (3.0 equivalents) were added. The mixture was heated to 110 °C in a single mode microwave reactor. Then it was poured into water and extracted with 3 portions of MTBE. The organic extract was dried over anhydrous sodium sulfate, evaporated and purified by chromatography on silica gel with a gradient of cyclohexane-ethyl acetate to give the title compound. General Synthetic Method 3 Mitsunobu Reaction A substituted (pyrazin-2-yl)ethan-1-ol (1 equivalent) was dissolved in THF (ca 3.0 mL/mmol ), 1H- isoindole-1,3(2H)-dione (1.50 equivalents) and triphenylphosphine (1.50 equivalents) were added. The mixture was cooled to 0 °C, then DIAD (1.50 equivalents) was slowly added and the mixture was left stirring for another 30 min. The solvent was distilled and the crude product was purified by preparative HPLC (RP C-18, water acetonitrile gradient with 0.1% TFA) to give the title compound. General Synthetic Method 4 Hydrazinolysis of phthalimide group A phthalimide protected amine (1 equivalent) was dissolved in ethanol (ca 10 mL/mmol) and hydrazine hydrate (80 % in water, 5 equivalents) was added. The mixture was heated to reflux for 1 h, then poured into water and extracted with 3 portions of dichloromethane. The organic phases were combined, dried over anhydrous sodium sulfate and evaporated. Optionally, the crude product was purified by flash chromatography to give the pure title compound. General Synthetic Method 5 Amide Coupling An amine (1.0 equivalents), a carboxylic acid (1.3 equivalents) and DIPEA (3.0 equivalents) were dissolved in DMF (ca 0.17 mmol amine per mL of DMF). The solution was cooled on an ice-water bath to 0 °C and HATU (1.5 equivalents) was added. The cooling bath was removed and mixture was stirred for 30 min. Then water was added. The precipitated product was collected on a filter funnel, dried under vacuum and eventually purified by preparative HPLC (RP-C18, water-acetonitril gradient with 0.1% TFA). General Synthetic Method 6 Copper Catalysed Coupling of Azoles (rac)-1-(3-Bromopyrazin-2-yl)ethan-1-ol (intermediate 22A, 1 equivalent) was dissolved in toluene (3.0 mL / 1.0 mmol of bromopyrazine), an azole (1.5 equivalents), potassium carbonate (2.5 equivalents), copper(I) iodide (0.3 equivalents) and trans- N,N,N',N'-tetramethylcyclohexane-1,2-diamine (0.3 equivalents) were added. The mixture was heated to reflux for 1 h and then poured into water. It was extracted with three portions of ethyl acetate, the combined organic extracts were washed twice with 20% aqueous ammonia, once with water and eventually once with brine. The organic phase was dried over anhydrous sodium sulfate, evaporated and the residue was purified on silica gel with a gradient of cyclohexane – ethyl acetate. Optionally, the crude product was once more purified by preparative HPLC (RP-C18 column with a water-acetonitrile gradient with 0.1% TFA) to give the title compound. SYNTHETIC INTERMEDIATES Intermediate 1A (rac)1-(3-Chloropyrazin-2-yl)ethan-1-ol
Figure imgf000111_0001
The reaction was carried out under dry argon, in flame-dried glassware.2,2,6,6-Tetramethylpiperidine (11 mL, 65 mmol) was dissolved in THF and cooled to -78 °C on an acetone- dry ice bath. n- Butyllithium (2.5 M in hexane, 25 mL, 64 mmol) was added dropwise so that the temperature did not exceed -70 °C. Afterwards, stirring was maintained at -78 °C for 30 min. Then, 2-chloropyrazine (5.73 g, 50.0 mmol) was added dropwise and the mixture was stired for 1 h. After this time, acetaldehyde (5.6 mL, 100 mmol) was added and the mixture was allowed to warm to room temperature and stirred for another 4 h. The reaction mixture was poured into water and extracted with ethyl acetate. The organic extract was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The crude product was purified by chromatography on silica gel using a gradient of cyclohexane and 0-40% ethyl acetate. 4.60 g (100 % purity, 58 % yield) of the title compound were obtained. LC-MS (method 1): Rt = 0.51 min; low ionization observed. ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.415 (15.85), 1.431 (16.00), 1.989 (0.55), 5.076 (0.46), 5.092 (1.88), 5.108 (2.88), 5.124 (1.97), 5.140 (0.51), 5.399 (4.89), 5.414 (4.45), 8.436 (3.29), 8.442 (3.57), 8.661 (3.47), 8.667 (3.40). Intermediate 2A (rac)-2-[1-(3-Chloropyrazin-2-yl)ethyl]-1H-isoindole-1,3(2)-dione
Figure imgf000111_0002
(rac) 1-(3-Chloropyrazin-2-yl)ethan-1-ol (intermediate 1A, 4.60 g, 29.0 mmol) was dissolved in THF (110 mL), 1H-isoindole-1,3(2H)-dione (6.40 g, 43.5 mmol) and triphenylphosphine (11.4 g, 43.5 mmol) were added at room temperature, then the mixture was cooled on an ice bath and DIAD (7.8 mL, 95 % purity, 44 mmol) was slowly added. The reaction was allowed to warm to ambient temperature and was stirred for 2 h. The solvent was distilled and the residue was directly charged onto a silica gel column (100 g of silica gel) and chromatographed using a gradient of cyclohexane and 0-35% ethyl acetate.5.37 g (98 % purity, 63 % yield) of the title compound were obtained. LC-MS (method 2): Rt = 1.69 min; MS (ESIpos): m/z = 288 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.208 (0.56), 1.219 (0.86), 1.231 (0.50), 1.793 (5.84), 1.805 (5.93), 5.696 (0.41), 5.708 (1.33), 5.720 (1.34), 5.731 (0.43), 7.868 (16.00), 8.490 (2.02), 8.494 (2.14), 8.702 (2.31), 8.706 (2.29). Intermediate 3A (rac)-2-{1-[3-(Pyridin-2-yl)pyrazin-2-yl]ethyl}-1-isoindole-1,3(2H)-dione
Figure imgf000112_0001
The reaction was carried out under dry argon, in flame-dried glassware. Preparation of the organozinc reagent (solution A) was carried out as described in M.R. Luzung, J.S. Patel, J. Yin, J. Org. Chem.2010, 75, 8330-8332. Solution A: A three-neck round-bottom flask with a stirbar was charged with isopropylmagnesium chloride (2.0 M in THF, 2.75 mL, 5.5 mmol). To this mixture was added neat 2-bromopyridine (0.476 mL, 5.0 mmol, 1.0 equiv) dropwise with the temperature not exceeding 30 °C. The mixture was stirred at room temperature for 3 h. Then, zinc chloride (1,9 M in THF, 3.16 mL, 6.0 mmol,) was added dropwise with the temperature not exceeding 30 °C and stirring was continued at room temperature for another 60 min.This solution was used as is for the subsequent cross coupling reaction. Solution B: Pd2(dba)3 (18.3 mg, 20.0 µmol) and dicyclohexyl[2',4',6'-tri(propan-2-yl)biphenyl-2- yl]phosphane (XPhos, 38.1 mg, 80.0 µmol) were dissolved in THF (2.0 mL). This mixture was heated to 65 °C for 10 min, then (rac)-2-[1-(3-chloropyrazin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (intermediate 2A, 288 mg, 1.00 mmol) was added and stirring at 65 °C was continued for another 15 min. Eventually, an aliquot of solution A (2.0 mL, 1.5 mmol) was added at once to solution B and the mixture was stirred at 65 °C for 7 h. Water (3.0 mL) and conc.aqueous sodium hydrogen carbonate (3.0 mL) were added, the mixture was extracted with ethyl acetate, the organic extract was washed with brine, dried over anhydrous sodium sulfate and evaporated. The crude product was purified by preparative HPLC using RP C-1810µm material and a gradient of water (+0.1% TFA) – acetonitrile (+0,1%TFA) 90:10->5:95). 219 mg (99 % purity, 66 % yield) of the title compound were obtained. LC-MS (method 2): Rt = 1.51 min; MS (ESIpos): m/z = 331 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.700 (15.91), 1.712 (16.00), 5.747 (3.09), 6.358 (1.15), 6.369 (3.78), 6.381 (3.73), 6.393 (1.13), 7.345 (2.24), 7.358 (2.63), 7.366 (2.41), 7.714 (4.89), 7.719 (5.36), 7.723 (6.03), 7.728 (7.85), 7.735 (1.21), 7.757 (3.00), 7.773 (10.68), 7.778 (6.32), 7.782 (5.81), 7.787 (5.19), 7.796 (2.95), 7.809 (3.67), 7.822 (1.46), 8.542 (3.70), 8.550 (3.71), 8.666 (4.22), 8.669 (8.32), 8.677 (7.99). Intermediate 4A (rac)-1-[3-(Pyridin-2-yl)pyrazin-2-yl]ethan-1-amine
Figure imgf000113_0001
(rac)-2-{1-[3-(Pyridin-2-yl)pyrazin-2-yl]ethyl}-1H-isoindole-1,3(2H)-dione (intermediate 3A, 218 mg, 660 µmol) was dissolved in ethanol (3.3 mL), hydrazine hydrate (160 µl, 3.3 mmol) was added and the mixture was heated to reflux for 2 h. The solvent was evaporated, ethyl acetate was added and the mixture was stirred at room temperature for 30 min. The precipitate was filtered off and the filtrate was evaporated. The crude title compound (143 mg (87 % purity, 94 % yield) was used in the next step without further purification. LC-MS (method 3): Rt = 0.92 min; MS (ESIneg): m/z = 199 [M-H]- ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.035 (0.48), 1.046 (0.48), 1.107 (1.71), 1.177 (0.45), 1.188 (0.44), 1.416 (15.78), 1.428 (16.00), 1.745 (4.66), 2.070 (3.46), 3.078 (0.63), 3.309 (1.12), 3.395 (0.61), 4.898 (0.98), 4.909 (3.05), 4.920 (3.04), 4.931 (1.00), 7.529 (1.82), 7.533 (1.81), 7.537 (1.96), 7.540 (2.67), 7.544 (2.03), 7.548 (1.92), 7.552 (1.89), 8.016 (0.84), 8.019 (0.84), 8.030 (3.14), 8.033 (3.26), 8.041 (7.28), 8.043 (6.99), 8.052 (0.99), 8.709 (6.08), 8.713 (7.38), 8.725 (2.35), 8.727 (3.04), 8.729 (2.35), 8.733 (2.36), 8.735 (3.49), 8.737 (2.14), 8.749 (6.63), 8.753 (5.60). Intermediate 5A (rac)-2-(1-(3-(Thiazol-2-yl)pyrazin-2-yl)ethyl)isoindoline-1,3-dione
Figure imgf000114_0001
To a solution of (rac)-2-[1-(3-chloropyrazin-2-yl)ethyl]-1H-isoindole-1,3(2)-dione (intermediate 2A, 1.2 g, 4.17 mmol), dichlorobis(triphenylphosphine)palladium(II) (293 mg, 0.42 mmol) in N,N- dimethylformamide (24 mL) was added 2-(tributylstannyl)thiazole (1.9 g, 5.01 mmol) at room temperature under N2 atmosphere. The resulting mixture was stirred at 85 °C overnight under N2 atmosphere. After cooled to room temperature, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was purified by silica gel chromatography (ethyl acetate: petroleum ether = 1:3) to afford 512 mg (31% purity) of the product as a white solid. LC-MS (method 6, gradient 0.01-1.50 min 5-100% B): Rt = 0.873 min; MS (ESIpos): m/z = 337 [M+H]+. Intermediate 6A (rac)-1-(3-(Thiazol-2-yl)pyrazin-2-yl)ethan-1-amine;
Figure imgf000114_0002
To a solution of (rac)-2-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)isoindoline-1,3-dione (intermediate 5A, 520 mg, 0.48 mmol, 31% purity) in ethanol (8 mL) was added hydrazine monohydrate (120 mg, 2.40 mmol). The resulting mixture was stirred at 95 °C for 2 h. After cooled to the room temperature, the solvent was removed in vacuo, ethyl acetate was added and the solution was stirring for 30 min. Then the solid was filtered out, the filtrate was concentrated to give 300 mg of the crude product as a yellow solid. LC-MS (method 6, gradient 0.01-1.50 min 5-100% B): Rt = 0.572 min; MS (ESIpos): m/z = 207 [M+H]+. Intermediate 7A 5-tert-Butylnicotinic acid
Figure imgf000115_0001
To a solution of 5-bromonicotinic acid (4.0 g, 19.99 mmol) and copper(I) iodide (380 mg, 2.00 mmol) in tetrahydrofuran (100 mL) was added a solution of tert-butylmagnesium chloride in tetrahydrofuran (1.7 M, 29.4 mL, 50.0 mmol) dropwise at -70 °C under N2 atmosphere. Then the mixture was stirred overnight at room temperature. The reaction was quenched by careful addition of ammonium chloride solution. The resulting mixture was concentrated and poured into water, then extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel chromatography to give 80 mg of desired product as a white solid. LC-MS (method 4, gradient 0.01-2.50 min 5-100% B): Rt = 0.718 min; MS (ESIpos): m/z = 180 [M+H]+. Intermediate 8A (rac)-2-(1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethyl)isoindoline-1,3-dione
Figure imgf000115_0002
To a solution of (rac)-2-[1-(3-Chloropyrazin-2-yl)ethyl]-1H-isoindole-1,3(2)-dione (intermediate 2A, 1.3 g, 4.52 mmol) in N,N-dimethylformamide (39 mL) was added Pd(AMPhos)2Cl2 (CAS RN 887919- 35-9, 0.3 g, 0.45 mmol), ZnCl2 (0.6 g, 4.52 mmol) and 2-(tributylstannyl)pyrimidine (2.5 g, 6.78 mmol) under N2 atmosphere. The resulting mixture was stirred overnight at 120 °C. After cooled to room temperature, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined and concentrated under vacuum. The residue was purified by silica gel chromatography (ethyl acetate: petroleum ether = 1:5) to afford 600 mg of the product (40% yield) as a white solid. Intermediate 9A (rac)-1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine
Figure imgf000116_0001
To a solution of rac-2-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)isoindoline-1,3-dione (intermediate 8A, 600 mg, 1.81 mmol) in ethanol (8 mL), was added hydrazine monohydrate (453 mg, 9.05 mmol). The resulting mixture was stirred at 95 °C for 2 h. After cooled to the room temperature, the solvent was removed in vacuo, Ethyl acetate was added and the solution was stirring for 30 min. Then the solid filtered out, the filtrated was concentrated to give 312 mg (85%) of the crude product as a yellow solid. LC-MS (method 4, gradient 0.01-1.80 min 5-100% B): Rt = 0.457 min; MS (ESIpos): m/z = 202 [M+H]+. Intermediate 10A 2-(5-Chloropyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
Figure imgf000116_0002
According to General Synthetic Method 1, 13.6 g (100 % purity, 49 % yield) of the title compound were synthesized from 2-bromo-5-chloropyridine (20.0 g, 104 mmol) obtained as crystalline solid. LC-MS (method 2): Rt = 0.96 min; MS (ESIpos): m/z = 269 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.106 (16.00), 1.122 (0.51), 2.823 (0.67), 3.077 (4.92), 4.060 (2.24), 4.102 (2.85), 4.376 (2.77), 4.419 (2.18), 7.572 (1.12), 7.592 (1.29), 7.862 (0.88), 7.868 (0.88), 7.882 (0.78), 7.888 (0.77), 8.724 (1.09), 8.729 (1.07). Other MIDA boronates prepared by General Synthetic Method 1: Intermediate 11A 6-Methyl-2-[5-(trifluoromethyl)pyridin-2-yl]-1,3,6,2-dioxazaborocane-4,8-dione
Figure imgf000117_0001
According to General Synthetic Method 1, 2.56 g (100 % purity, 38 % yield) of the title compound were synthesized from 2-bromo-5-trifluoromethylpyridine (5.00 g, 22.1 mmol) obtained as crystalline solid. LC-MS (method 2): Rt = 1.19 min; MS (ESIpos): m/z = 303 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 0.871 (0.42), 0.884 (0.42), 1.107 (3.20), 1.121 (1.66), 2.575 (16.00), 2.783 (1.36), 2.800 (0.66), 2.826 (0.55), 2.919 (2.76), 3.078 (0.89), 3.995 (0.46), 4.024 (0.68), 4.103 (5.55), 4.132 (6.70), 4.157 (0.77), 4.167 (1.28), 4.187 (0.57), 4.196 (1.58), 4.342 (1.31), 4.370 (0.96), 4.417 (6.51), 4.445 (5.50), 7.790 (2.61), 7.804 (2.83), 8.142 (2.22), 8.155 (2.13), 9.052 (3.80). Intermediate 12A 2-(5-Methoxypyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
Figure imgf000117_0002
According to General Synthetic Method 1, 3.25 g (95 % purity, 22 % yield) of the title compound were synthesized from 2-bromo-5-methoxypyridine (10.0 g, 53.2 mmol) obtained as crystalline solid. LC-MS (method 3): Rt = 0.88 min; MS (ESIpos): m/z = 265 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 2.514 (13.24), 2.663 (1.41), 3.823 (16.00), 3.824 (15.35), 3.844 (1.76), 4.032 (4.59), 4.061 (5.40), 4.333 (5.36), 4.362 (4.47), 4.392 (0.52), 4.420 (0.44), 7.305 (1.32), 7.308 (1.37), 7.318 (1.53), 7.322 (1.56), 7.474 (0.57), 7.488 (2.76), 7.502 (2.35), 8.140 (0.56), 8.407 (2.61), 8.411 (2.53). Intermediate 13A (rac)-1-[3-(5-Chloropyridin-2-yl)pyrazin-2-yl]ethan-1-ol
Figure imgf000118_0001
According to General Synthetic Method 2, 410 mg (96 % purity, 17 % yield) of the title compound were obtained from (rac)-1-(3-bromopyrazin-2-yl)ethan-1-ol (2.00 g, 9.85 mmol) and 2-(5- chloropyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (intermediate 10A, 3.31 g, 96 % purity, 11.8 mmol). LC-MS (method 9): Rt = 0.72 min; MS (ESIpos): m/z = 236 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.439 (5.75), 1.449 (5.77), 3.289 (16.00), 5.164 (1.86), 5.175 (2.20), 5.283 (0.97), 5.294 (1.39), 5.304 (0.88), 8.005 (1.56), 8.019 (1.94), 8.132 (1.18), 8.136 (1.20), 8.146 (0.99), 8.150 (0.99), 8.666 (1.85), 8.670 (2.07), 8.728 (2.02), 8.732 (1.83), 8.771 (1.74), 8.775 (1.72). Intermediate 14A (rac)-1-{3-[5-(Trifluoromethyl)pyridin-2-yl]pyrazin-2-yl}ethan-1-ol
Figure imgf000118_0002
According to General Synthetic Method 2, 736 mg (98 % purity, 35 % yield) of the title compound were obtained from (rac)-1-(3-bromopyrazin-2-yl)ethan-1-ol (1.55 g, 7.63 mmol) and 6-Methyl-2-[5- (trifluoromethyl)pyridin-2-yl]-1,3,6,2-dioxazaborocane-4,8-dione (intermediate 11A, 2.65 g, 8.78 mmol). LC-MS (method 2): Rt = 1.46 min; MS (ESIpos): m/z = 270 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.463 (16.00), 1.474 (16.00), 4.337 (0.42), 5.296 (1.07), 5.307 (3.14), 5.318 (3.12), 5.328 (1.05), 8.175 (2.20), 8.189 (2.47), 8.412 (2.79), 8.415 (2.76), 8.426 (2.55), 8.428 (2.50), 8.713 (3.36), 8.780 (3.42), 9.116 (3.28). Intermediate 15A (rac)-1-[3-(5-Methoxypyridin-2-yl)pyrazin-2-yl]ethan-1-ol
Figure imgf000119_0001
According to General Synthetic Method 2, 480 mg (100 % purity, 44 % yield) of the title compound were obtained from (rac)-1-(3-bromopyrazin-2-yl)ethan-1-ol (961 mg, 4.73 mmol) and 2-(5- Methoxypyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione (intermediate 12A, 1.50 g, 5.68 mmol). LC-MS (method 2): Rt = 1.12 min; MS (ESIpos): m/z = 232 [M+H]+ ¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 1.434 (6.13), 1.447 (6.14), 3.824 (0.47), 3.927 (16.00), 5.244 (0.96), 5.256 (1.47), 5.269 (0.99), 5.504 (2.39), 5.517 (2.16), 7.614 (1.28), 7.620 (1.29), 7.632 (1.38), 7.638 (1.39), 8.016 (2.04), 8.033 (1.85), 8.439 (1.91), 8.444 (1.84), 8.633 (2.32), 8.638 (3.22), 8.659 (2.97), 8.664 (2.08). Intermediate 16A (rac)-2-{1-[3-(5-Chloropyridin-2-yl)pyrazin-2-yl]ethyl}-1H-isoindole-1,3(2H)-dione
Figure imgf000119_0002
According to General Synthetic Method 3, 458 mg (100 % purity, 72 % yield) of the title compound were obtained from (rac)-1-[3-(5-chloropyridin-2-yl)pyrazin-2-yl]ethan-1-ol (intermediate 13A, 410 mg, 1.74 mmol). LC-MS (method 2): Rt = 1.91 min; MS (ESIpos): m/z = 365 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.171 (0.62), 1.187 (0.72), 1.201 (0.57), 1.217 (0.50), 1.709 (15.98), 1.727 (16.00), 1.739 (0.74), 1.757 (0.48), 2.072 (0.99), 6.275 (1.08), 6.292 (4.05), 6.310 (4.02), 6.327 (1.07), 7.726 (4.85), 7.733 (5.58), 7.740 (4.92), 7.747 (9.26), 7.757 (1.56), 7.778 (2.12), 7.788 (9.71), 7.797 (5.84), 7.801 (9.05), 7.809 (5.73), 7.821 (5.58), 7.830 (0.77), 7.924 (4.64), 7.931 (4.68), 7.946 (3.38), 7.952 (3.50), 8.571 (3.68), 8.577 (3.67), 8.698 (15.93), 8.704 (2.65). Intermediate 17A (rac)-2-[1-{3-[5-(Trifluoromethyl)pyridin-2-yl]pyrazin-2-yl}ethyl]-1H-isoindole-1,3(2H)-dione
Figure imgf000120_0001
According to General Synthetic Method 3, 897 mg (100 % purity, 82 % yield) of the title compound were obtained from (rac)-1-{3-[5-(trifluoromethyl)pyridin-2-yl]pyrazin-2-yl}ethan-1-ol (intermediate 14A, 736 mg, 2.73 mmol). LC-MS (method 2): Rt = 1.99 min; MS (ESIpos): m/z = 399 [M+H]+
Intermediate 18A (rac)-2-{1-[3-(5-methoxypyridin-2-yl)pyrazin-2-yl]ethyl}-1H-isoindole-1,3(2H)-dione
Figure imgf000121_0001
According to General Synthetic Method 3, 325 mg (97 % purity, 88 % yield) of the title compound were obtained from (rac)-1-[3-(5-methoxypyridin-2-yl)pyrazin-2-yl]ethan-1-ol (intermediate 15A, 230 mg, 1.00 mmol). LC-MS (method 2): Rt = 1.65 min; MS (ESIpos): m/z = 361 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.164 (0.74), 1.176 (2.18), 1.188 (2.01), 1.709 (6.41), 1.721 (6.32), 1.988 (1.52), 3.820 (16.00), 6.399 (0.46), 6.411 (1.51), 6.423 (1.49), 6.435 (0.44), 7.399 (1.31), 7.404 (1.33), 7.414 (1.41), 7.419 (1.40), 7.550 (0.84), 7.555 (0.69), 7.562 (0.69), 7.567 (0.58), 7.606 (0.87), 7.611 (0.49), 7.618 (0.69), 7.625 (1.26), 7.639 (0.82), 7.741 (1.97), 7.746 (2.26), 7.750 (2.33), 7.755 (3.40), 7.762 (0.55), 7.781 (0.63), 7.788 (3.47), 7.793 (2.38), 7.797 (2.30), 7.802 (2.07), 7.807 (2.62), 7.822 (2.27), 8.259 (2.29), 8.263 (2.25), 8.588 (2.48), 8.592 (2.89), 8.631 (2.64), 8.635 (2.25). Intermediate 19A (rac)-1-[3-(5-Chloropyridin-2-yl)pyrazin-2-yl]ethan-1-amine
Figure imgf000121_0002
According to General Procedure 4, 285 mg (100 % purity, 97 % yield) of the title compound were obtained from (rac)-2-{1-[3-(5-chloropyridin-2-yl)pyrazin-2-yl]ethyl}-1-isoindole-1,3(2H)-dione (intermediate 16A, 457 mg, 1.25 mmol). LC-MS (method 2): Rt = 0.69 min; MS (ESIpos): m/z = 235 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.178 (1.08), 1.188 (1.03), 1.235 (0.56), 1.335 (15.63), 1.346 (16.00), 1.542 (0.57), 1.554 (0.54), 3.239 (2.07), 4.581 (0.99), 7.880 (0.43), 7.995 (9.27), 8.009 (11.43), 8.061 (0.42), 8.070 (0.50), 8.127 (7.67), 8.131 (7.76), 8.141 (6.36), 8.146 (6.35), 8.633 (4.91), 8.667 (0.45), 8.671 (0.50), 8.724 (2.87), 8.769 (10.46), 8.773 (10.19). Intermediate 20A (rac)-1-{3-[5-(Trifluoromethyl)pyridin-2-yl]pyrazin-2-yl}ethan-1-amine
Figure imgf000122_0001
According to General Procedure 4, 600 mg (94 % purity, 94 % yield) of the title compound were obtained from (rac)-2-[1-{3-[5-(trifluoromethyl)pyridin-2-yl]pyrazin-2-yl}ethyl]-1H-isoindole-1,3(2H)- dione (intermediate 17A, 895 mg, 2.25 mmol). LC-MS (method 2): Rt = 0.83 min; MS (ESIpos): m/z = 269 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: -0.149 (0.45), 0.146 (0.47), 1.150 (0.53), 1.157 (0.64), 1.174 (1.96), 1.188 (1.70), 1.338 (15.76), 1.355 (16.00), 1.988 (1.27), 2.082 (1.11), 2.710 (0.40), 4.485 (0.83), 4.502 (2.44), 4.518 (2.42), 4.534 (0.82), 8.166 (3.45), 8.187 (4.18), 8.410 (2.44), 8.416 (2.48), 8.431 (2.19), 8.436 (2.21), 8.664 (5.15), 8.669 (5.67), 8.767 (5.57), 8.773 (5.03), 9.121 (3.56), 9.123 (3.60). Intermediate 21A (rac)-1-[3-(5-Methoxypyridin-2-yl)pyrazin-2-yl]ethan-1-amine
Figure imgf000122_0002
According to General Procedure 4, 220 mg (60 % purity, 64 % yield) of the title compound were obtained from (rac)-2-[1-{3-[5-(methoxy)pyridin-2-yl]pyrazin-2-yl}ethyl]-1H-isoindole-1,3(2H)-dione (intermediate 18A, 325 mg, 0.90 mmol). LC-MS (method 2): Rt = 0.60 min; MS (ESIpos): m/z = 321 [M+H]+ Intermediate 22A (rac)-1-(3-Bromopyrazin-2-yl)ethan-1-ol
Figure imgf000123_0001
A solution of 2,2,6,6-tetramethylpiperidine (21 mL, 120 mmol) in THF (260 mL) was cooled to -78 °C. A solution of n-butyllithium (2.5 M in hexanes, 48 mL, 120 mmol) was slowly added and stirring was maintained for 30 min at -78 °C. Then, 2-bromopyrazine (8.5 mL, 94 mmol) was added dropwise keeping the temperature at -70 °C. Stirring was continued at -78 °C for one hour. Acetaldehyde (11 mL, 190 mmol) was added dropwise, the cooling bath was removed and the mixture was allowed to slowly warm to room temperature. The reaction mixture was poured into water (500 mL), acidified with 1 M hydrochloric acid and extracted with 6 portions of ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, the solvent was carefully distilled (40 °C bath temperature, 140 mbar) on the rotatory evaporator and eventually purified by flash chromatography on silica gel with a gradient of cyclohexane-ethyl acetateto yield 12.6 g (61% of theory) of the title compound. LC-MS (method 2): Rt = 0.81 min; MS (ESIpos): m/z = 203 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.164 (2.79), 1.176 (5.67), 1.187 (2.84), 1.407 (15.63), 1.418 (16.00), 1.907 (0.49), 1.987 (10.52), 4.013 (0.83), 4.025 (2.50), 4.037 (2.49), 4.049 (0.82), 5.076 (0.53), 5.087 (2.14), 5.097 (3.28), 5.108 (2.23), 5.119 (0.58), 5.353 (5.76), 5.363 (5.33), 5.744 (1.31), 8.400 (4.78), 8.404 (4.96), 8.670 (4.87), 8.674 (4.75). Intermediate 23A (rac)-2-[1-(3-bromopyrazin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione
Figure imgf000123_0002
According to General synthetic method 3, 12.8 g (98 % purity, 77 % yield) was obtained from (rac)-1- (3-bromopyrazin-2-yl)ethan-1-ol (intermediate 22A, 10.0 g, 49.3 mmol). LC-MS (method 2): Rt = 1.75 min; MS (ESIpos): m/z = 332 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.179 (0.88), 1.189 (0.84), 1.786 (5.16), 1.798 (5.17), 5.655 (1.17), 5.667 (1.14), 7.867 (16.00), 8.452 (1.85), 8.457 (1.83), 8.708 (2.09), 8.712 (1.94). Intermediate 24A (rac)-Methyl 6-{3-[-1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]pyrazin-2-yl}pyridine-3- carboxylate
Figure imgf000124_0001
Solution A - chlorido[5-(methoxycarbonyl)pyridin-2-yl]zinc in THF: In a flame-dried 3-neck round bottom flask, methyl 6-iodopyridine-3-carboxylate (1.88 g, 7.15 mmol) was suspended in THF (8.0 mL) and then cooled to -30 °C.A solution of isopropylmagnesium chloride x lithium chloride (1,3 M in THF, 7.1 mL, 9.3 mmol) was added dropwise and the mixture was stirred for 5 min. Then, zinc dichloride (4.5 mL, 1.9 M in methyl-THF, 8.6 mmol) was added. This solution was then directly used for the cross coupling reaction. To this end, (rac)-2-[-(3-bromopyrazin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (intermediate 23A, 780 mg, 2.34 mmol) and 1,1-bis(diphenylphosphino)-ferrocenedichloropalladium(II) (192 mg, 234 µmol) were put in two separate microwave reactor vials under argon, solution A was added and the mixture was heated to 110 °C in a single mode microwave device for 90 min. After cooling, the mixture was charged upon silica gel, evaporated and then purified by flash chromatography with a gradient of cyclohexane – ethyl acetate to give 97.0 mg (97 % purity, 11 % yield) of the title compound. LC-MS (method 9): Rt = 0.92 min; MS (ESIpos): m/z = 389 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.719 (4.11), 1.731 (4.05), 2.069 (0.45), 3.289 (16.00), 3.901 (9.08), 3.934 (0.75), 6.306 (1.05), 6.318 (1.04), 7.690 (1.45), 7.696 (1.59), 7.699 (1.63), 7.705 (1.97), 7.764 (2.09), 7.769 (1.71), 7.773 (1.54), 7.778 (1.40), 7.912 (1.49), 7.926 (1.61), 8.247 (0.99), 8.250 (0.93), 8.260 (0.92), 8.264 (0.85), 8.726 (2.04), 8.738 (2.11), 8.742 (1.29), 8.985 (1.57), 8.987 (1.53). Intermediate 25A (rac)-Methyl 6-{3-[1-aminoethyl]pyrazin-2-yl}pyridine-3-carboxylate
Figure imgf000125_0001
According to General synthetic method 4, 115 mg (79 % purity, 85 % yield) were obtained from (rac)- methyl 6-{3-[1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]pyrazin-2-yl}pyridine-3-carboxylate (intermediate 24A, 160 mg, 412 µmol) LC-MS (method 2): Rt = 0.76 min; MS (ESIpos): m/z = 259 [M+H]+ Intermediate 26A (rac)-(6-{3-[1-Aminoethyl]pyrazin-2-yl}pyridin-3-yl)(morpholin-4-yl)methanone
Figure imgf000125_0002
Intermediate 27A (rac)-Methyl 2-{3-[1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]pyrazin-2-yl}-1,3-thiazole-5- carboxylate
Figure imgf000125_0003
Solution A: Methyl 2-bromo-1,3-thiazole-5-carboxylate (2.00 g, 9.00 mmol) was dissolved in THF (9.0 mL). The mixture was cooled to -40 °C and isopropylmagnesium chloride x lithium chloride (8.3 mL, 1.3 M in THF, 11 mmol) was added. The temperature was adjusted to -70 °C and a solution of zinc dichloride (5.2 mL, 1.9 M in methyl-THF, 9.9 mmol) was added keeping the temperature in a range between -50 and -70 °C. This solution was immediately used in the cross coupling reaction. (rac)-2-[1-(3-bromopyrazin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione (intermediate 23A, 950 mg, 2.86 mmol) was dissolved in THF (17.0 mL).1,1-Bis(diphenylphosphino)-ferrocenedichloropalladium(II): (117 mg, 143 µmol) and solution A were added. The resulting mixture was distributed into 20 mL microwave reactor vials under an argon atmosphere. Each vial was crimp-capped and heated to 120 °C for 2 h in a single mode microwave device. After cooling, the aliquots were combined, diluted with water (20 mL) and conc. aq. sodium hydrogen carbonate (20 mL) and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate, filtered and evaporated. The crude product was first purified by column chromatography (silica gel, cyclohexane ethyl acetate gradient with 0-35% etyl acetate) and eventually by preparative HPLC (RP-C18 column, water-acetonitril gradient with 0.1% TFA) to give 510 mg (100 % purity, 45 % yield) of the title compound. LC-MS (method 2): Rt = 2.04 min; MS (ESIpos): m/z = 395 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.106 (5.49), 1.892 (4.85), 1.904 (4.85), 3.077 (1.74), 3.886 (10.87), 6.653 (1.27), 6.665 (1.27), 7.839 (16.00), 8.610 (3.63), 8.730 (0.78), 8.735 (5.05), 8.740 (0.86). Intermediate 28A (rac)-Methyl 2-{3-[1-aminoethyl]pyrazin-2-yl}-1,3-thiazole-5-carboxylate
Figure imgf000126_0001
According to General synthetic method 4, (rac)-methyl 2-{3-[1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2- yl)ethyl]pyrazin-2-yl}-1,3-thiazole-5-carboxylate (intermediate 27A, 730 mg, 1.85 mmol) was converted into 300 mg (96 % purity, 59 % yield) of the title compound. LC-MS (method 3): Rt = 1.32 min; MS (ESIpos): m/z = 265 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.164 (0.49), 1.176 (0.98), 1.188 (0.50), 1.345 (7.54), 1.356 (7.35), 1.987 (1.84), 3.895 (16.00), 3.906 (0.60), 4.025 (0.43), 4.037 (0.43), 5.271 (0.52), 5.281 (1.71), 5.292 (1.70), 5.303 (0.52), 8.649 (5.41), 8.653 (3.03), 8.657 (3.10), 8.799 (2.80), 8.803 (2.77). Intermediate 29A (rac)-Ethyl 1-{3-[1-hydroxyethyl]pyrazin-2-yl}-1H-pyrazole-4-carboxylate
Figure imgf000127_0001
(rac)-1-(3-Bromopyrazin-2-yl)ethan-1-ol (intermediate 22A, 500 mg, 2.46 mmol) was dissolved in toluene (5.0 mL), ethyl 1H-pyrazole-4-carboxylate (518 mg, 3.69 mmol), potassium carbonate (851 mg, 6.16 mmol), copper(I) iodide (141 mg, 0.74 mmol) and trans- N,N,N',N'-tetramethylcyclohexane-1,2- diamine (120 µl, 740 µmol) were added. The mixture was heated to reflux for 1 h and then poured into water. It was extracted with three portions of ethyl acetate, the combined organic extracts were washed twice with 20% aqueous ammonia, once with water and eventually once with brine. The organic phase was dried over anhydrous sodium sulfate, evaporated and the residue was purified on silica gel with a gradient of cyclohexane – ethyl acetate. The crude product was once more purified by preparative HPLC (RP-C18 column with a water-acetonitrile gradient with 0.1% TFA) to give 389 mg (100 % purity, 60 % yield) of the title compound. LC-MS (method 2): Rt = 1.34 min; MS (ESIpos): m/z = 263 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.298 (7.89), 1.309 (16.00), 1.321 (7.95), 1.430 (14.41), 1.441 (14.34), 2.073 (1.32), 4.273 (2.53), 4.285 (7.54), 4.297 (7.46), 4.309 (2.39), 5.225 (1.14), 5.235 (3.55), 5.246 (3.47), 5.257 (1.07), 8.247 (7.91), 8.595 (5.44), 8.598 (5.53), 8.830 (5.44), 8.834 (5.22), 8.872 (8.46). In analogy, the following intermediates were synthesized according to General synthetic method 6:
Figure imgf000127_0002
Figure imgf000128_0001
Intermediate 33A (rac)-Ethyl 1-{3-[1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]pyrazin-2-yl}-1H-pyrazole-4- carboxylate
Figure imgf000129_0001
According to General synthetic method 3, (rac)-Ethyl 1-{3-[1-hydroxyethyl]pyrazin-2-yl}-1H-pyrazole- 4-carboxylate (intermediate 29A, 385 mg, 1.47 mmol) was converted into the title compound (500 mg, 100 % purity, 87 % yield). LC-MS (method 2): Rt = 1.91 min; MS (ESIpos): m/z = 392 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.165 (0.45), 1.177 (0.84), 1.189 (0.54), 1.260 (7.86), 1.271 (16.00), 1.283 (7.88), 1.397 (2.89), 1.666 (13.05), 1.678 (12.95), 1.989 (1.24), 4.212 (2.54), 4.224 (7.65), 4.236 (7.48), 4.248 (2.42), 5.747 (0.48), 6.202 (0.98), 6.214 (3.19), 6.226 (3.17), 6.237 (0.93), 7.789 (2.91), 7.795 (3.67), 7.799 (4.33), 7.804 (8.09), 7.811 (3.87), 7.818 (8.03), 7.824 (4.11), 7.827 (3.93), 7.832 (3.07), 8.100 (8.47), 8.633 (4.91), 8.637 (5.10), 8.776 (5.51), 8.780 (5.40), 8.790 (9.02). According to General synthetic method 3, the following intermediates were obtained:
Figure imgf000130_0001
Figure imgf000131_0002
Intermediate 37A (rac)-Ethyl 1-{3-[1-aminoethyl]pyrazin-2-yl}-1H-pyrazole-4-carboxylate
Figure imgf000131_0001
According to General synthetic method 4, (rac)-ethyl 1-{3-[1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2- yl)ethyl]pyrazin-2-yl}-1H-pyrazole-4-carboxylate (500 mg, 1.28 mmol) was transformed into 330 mg (96 % purity, 95 % yield) of the title compound. LC-MS (method 2): Rt = 0.76 min; MS (ESIpos): m/z = 262 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.296 (5.40), 1.308 (16.00), 1.321 (13.65), 2.001 (0.56), 4.272 (1.75), 4.283 (5.36), 4.295 (5.41), 4.307 (1.94), 4.396 (0.71), 4.407 (2.18), 4.418 (2.21), 4.429 (0.79), 8.246 (5.19), 8.539 (3.55), 8.543 (3.95), 8.806 (3.51), 8.810 (3.73), 8.853 (5.63). The following intermediates were synthesized according to General synthetic method 4:
Figure imgf000132_0001
Figure imgf000133_0003
Intermediate 41A (rac)-Methyl 2-(3-{1-[(tert-Butoxycarbonyl)amino]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylate
Figure imgf000133_0001
(rac)-Methyl 2-{3-[1-Aminoethyl]pyrazin-2-yl}-1,3-thiazole-5-carboxylate (intermediate 28A, 1.40 g, 5.30 mmol) was suspended in THF (30.0 mL), triethylamine (5.9 ml, 42.0 mmol) and di-tert-butyl dicarbonate (4.62 g, 21.2 mmol) were added at room temperature and the mixture was stirred for 1 h. The mixture was poured into water and extracted with three portions of ethyl acetate. The organic phase was dried over sodium sulfate and evaporated. The solid residue was triturated with MTBE, collected on a filter funnel and dried to give a first crop of the title compound 1.30 g (97 % purity, 65 % yield). The filtrate was evaporated and the residue purified by chromatography on silica gel (cyclohexane – ethyl acetate gradient) to yield a second crop 490 mg (100 % purity, 25 % yield) of the desired product. LC-MS (Method 2): Rt = 2.08 min; MS (ESIpos): m/z = 365 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 0.940 (1.20), 1.299 (13.37), 1.320 (0.58), 1.332 (0.45), 1.374 (3.69), 1.385 (3.89), 1.466 (1.76), 3.273 (0.43), 3.897 (16.00), 6.011 (1.33), 6.023 (1.99), 6.035 (1.36), 7.298 (0.73), 7.310 (0.69), 8.669 (7.68), 8.677 (3.66), 8.681 (3.76), 8.790 (1.45). Intermediate 42A (+)-Methyl 2-(3-{(1S)-1-[(tert-Butoxycarbonyl)amino]ethyl}pyrazin-2-yl)-1,3-thiazole-5- carboxylate
Figure imgf000133_0002
Both crops were combined and submitted to chiral preparative HPLC (stationary phase: Daicel Chiralpak IC 5µm 250x20 mm; mobile phase: n-heptane / ethanol 4:1; flow 25 mL/min. Isomer 1: 0.75 g (39% of theory) Analytical chiral HPLC (Method 14): Rt = 1.80 min. Isomer 2: 0.73 g (37% of theory) Analytical chiral HPLC (Method 14): Rt = 2.48 min. [α]D 20 = +92.4 ° (c = 0.37, CHCl3) Isomer 2 was further processed into the following synthetic steps. Intermediate 43A (+)-2-(3-{(1S)-1-[(tert-Butoxycarbonyl)amino]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid
Figure imgf000134_0001
(+)-Methyl 2-(3-{(1S)-1-[(tert-Butoxycarbonyl)amino]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylate (intermediate 42A, 730 mg, 2.00 mmol) was dissolved in THF (20.0 mL). Water (5.0 mL) was added, the mixture was cooled to 0 °C and lithium hydroxide (240 mg, 10.0 mmol) was added. The mixture was stirred 105 min at 0 °C, then it was diluted with water, acidified with 1M hydrochloric acid to pH 5 and extracted with 5 portions of ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated. The residue was dried under vacuum to give 709 mg (100 % purity, quant. yield) of the title compound. [α]D 20 = +92.3 ° (c = 0.35, CHCl3) LC-MS (Method 2): Rt = 1.53 min; MS (ESIpos): m/z = 351 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 0.954 (1.65), 1.165 (0.95), 1.177 (1.85), 1.188 (0.97), 1.307 (16.00), 1.357 (2.33), 1.375 (4.46), 1.386 (4.67), 1.750 (0.66), 1.756 (0.80), 1.761 (1.77), 1.767 (0.72), 1.772 (0.61), 1.990 (3.32), 3.403 (0.72), 3.592 (1.08), 3.614 (0.99), 4.025 (0.85), 4.037 (0.85), 6.020 (1.51), 6.032 (2.21), 6.044 (1.51), 7.256 (0.94), 7.268 (0.87), 8.435 (2.93), 8.657 (4.83), 8.661 (4.96), 8.750 (1.97). Intermediate 44A (+)-tert-Butyl [(1S)-1-(3-{5-[Ethyl(methyl)carbamoyl]-1,3-thiazol-2-yl}pyrazin-2- yl)ethyl]carbamate
Figure imgf000135_0001
(+)-2-(3-{(1S)-1-[(tert-Butoxycarbonyl)amino]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid (intermediate 43A, 825 mg, 2.35 mmol) was dissolved in DMF (19.0 mL) and the solution was cooled to 0 °C. N-Methylethanamine (300 µl, 3.5 mmol) and DIPEA (1.6 ml, 9.4 mmol) were added followed by HATU (1.79 g, 4.71 mmol), the mixture was allowed to warm to ambient temperature and stirred for 40 min. The mixture was directly charged upon a RP-18 HPLC column and chromatographed (RP C-18 10µm ACN:water +0,1%TFA 10:90->95:5) to yield 880 mg (100 % purity, 95 % yield) of the title compound. [α]D 20 = +72.6 ° (c = 0.22, CHCl3) LC-MS (Method 2): Rt = 1.84 min; MS (ESIpos): m/z = 392 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 0.952 (1.46), 1.176 (1.74), 1.307 (16.00), 1.380 (5.16), 1.397 (5.30), 3.011 (0.61), 3.218 (0.75), 3.502 (1.77), 3.519 (1.72), 6.022 (1.07), 6.040 (1.66), 6.058 (1.15), 7.282 (0.81), 7.300 (0.77), 8.652 (3.72), 8.658 (4.27), 8.753 (1.91).
Figure imgf000135_0002
Figure imgf000136_0001
Figure imgf000137_0002
Intermediate 48A (-)-2-{3-[(1S)-1-Aminoethyl]pyrazin-2-yl}-N-Ethyl-N-methyl-1,3-thiazole-5-carboxamide hydrogen chloride
Figure imgf000137_0001
(+)-tert-Butyl [(1S)-1-(3-{5-[Ethyl(methyl)carbamoyl]-1,3-thiazol-2-yl}pyrazin-2-yl)ethyl]carbamate (intermediate 44A, 875 mg, 2.24 mmol) was dissolved in a solution of hydrogen chloride (4.0 m in1,4- dioxane, 9.6 mL, 38 mmol) and the mixture was stirred at room temperature for 30 min. Then volatile components were distilled and the residue was dried under vacuum.729 mg (100 % purity, 99 % yield) of the title compound were obtained. [α]D20 = -43.8 ° (c = 0.21, water) LC-MS (Method 2): Rt = 0.72 min; MS (ESIpos): m/z = 292 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: -0.149 (0.44), 0.146 (0.44), 1.179 (3.64), 1.560 (15.78), 1.576 (16.00), 2.368 (0.52), 2.712 (0.52), 3.014 (1.48), 3.213 (2.00), 3.482 (2.41), 3.500 (7.02), 3.518 (6.88), 3.536 (2.34), 3.568 (2.45), 5.761 (1.73), 5.776 (2.28), 5.791 (1.72), 8.480 (6.02), 8.837 (6.80), 8.843 (9.10), 8.877 (8.80), 8.883 (7.02).
Figure imgf000137_0003
Figure imgf000138_0001
Figure imgf000139_0001
Examples Example I-1 (rac)-3-Chloro-N-{1-[3-(pyridin-2-yl)pyrazin-2-yl]ethyl}-5-(trifluoromethyl)benzamide
Figure imgf000140_0001
(rac)-1-[3-(Pyridin-2-yl)pyrazin-2-yl]ethan-1-amine (intermediate 4A, 66.1 mg, 330 µmol) was dissolved in DMF (3.5 mL), HATU (188 mg, 495 µmol), 3-chloro-5-(trifluoromethyl)benzoic acid (81.5 mg, 363 µmol) and DIPEA (170 µl, 990 µmol) were added and the mixture was stirred at room temperature for 45 min. The reaction mixture was directly charged onto a preparative HPLC and purified using RP C-1810µm material and a gradient water (+0.1% TFA) – acetonitrile (+0.1% TFA) 90:10->5:95). 67.0 mg (94 % purity, 47 % yield) of the title compound were obtained. LC-MS (method 1): Rt = 1.37 min; MS (ESIpos): m/z = 407 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: 1.640 (15.92), 1.657 (16.00), 2.328 (0.59), 2.367 (0.88), 2.671 (0.57), 2.711 (0.89), 5.802 (0.55), 5.819 (2.55), 5.837 (3.96), 5.854 (2.52), 5.871 (0.53), 7.488 (2.24), 7.499 (4.50), 7.509 (4.34), 7.521 (2.44), 7.994 (8.18), 7.998 (9.32), 8.007 (8.65), 8.010 (5.11), 8.019 (4.70), 8.070 (5.99), 8.125 (5.81), 8.189 (0.88), 8.645 (7.54), 8.651 (9.96), 8.686 (9.02), 8.692 (6.94), 8.709 (2.63), 8.712 (4.56), 8.715 (2.62), 8.721 (2.72), 8.724 (4.10), 8.727 (2.43), 9.221 (3.27), 9.239 (3.22). Example I-2 (rac)-N-(1-(3-(Thiazol-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)nicotinamide
To a solution of (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A, 100 mg, 0.49 mmol) in N,N-dimethylformamide (8 mL) was added 5-(trifluoromethyl)nicotinic acid (93 mg, 0.49 mmol), HATU (277 mg, 0.73 mmol), and N,N-diisopropylethylamine (188 mg, 1.45 mmol). The resulting mixture was stirred at room temperature overnight. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrate under vacuum. The residue was purified by Prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3 .H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 60 B to 80 B in 7 min] to give 9.9 mg (98% purity, 5.28% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.60-1.62 (d, 3H), 6.53-6.60 (m, 1H), 8.02-8.03 (d, 1H), 8.16-8.17 (d, 1H), 8.64-8.66 (m, 2H), 8.70-8.71 (d, 1H), 9.12-9.13 (d, 1H), 9.24-9.25 (d, 1H), 9.48-9.50 (d, 1H). LC-MS (method 4, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.340 min; MS (ESIpos): m/z = 380 [M+H]+. Example I-3 (rac)-3-Chloro-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
Figure imgf000141_0001
To a solution of (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A,100 mg, 0.49 mmol) in N,N-dimethylformamide (8 mL) was added 3-chloro-5-(trifluoromethyl)benzoic acid (109 mg, 0.49 mmol), HATU (277 mg, 0.73 mmol), and N,N-diisopropylethylamine (188 mg, 1.45 mmol). The resulting mixture was stirred at room temperature overnight. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by Prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3 .H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 65 B to 95 B in 7 min] to give 16.50 mg (99% purity, 8.2% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.59-1.61 (d, 3H), 6.49-6.56 (m, 1H), 8.02-8.03 (d, 1H), 8.07 (d, 1H), 8.15-8.16 (d, 1H), 8.19 (d, 1H), 8.24 (d, 1H), 8.64-8.66 (d, 1H), 8.69-8.70 (d, 1H), 9.40- 9.42 (d, 1H). LC-MS (method 5, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.848 min; MS (ESIpos): m/z = 413 [M+H]+. Example I-4 (rac)-3-Fluoro-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
Figure imgf000142_0001
To a solution of (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A,160 mg, 0.23 mmol) in dichloromethane (8 mL) was added 3-fluoro-5-(trifluoromethyl)benzoyl chloride (58 mg, 0.26 mmol), and triethylamine (71 mg, 0.70 mmol). The resulting mixture was stirred at room temperature overnight. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by Prep- HPLC with the following conditions [Column: Mobile Phase A: Water (0.1% FA), Mobile Phase B: ACN; Flow rate: 60 mL/min; Gradient: 52 B to 69 B in 8 min] to give 17.80 mg (97% purity, 18.7% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.59-1.61 (d, 3H), 6.51-6.55 (m, 1H), 7.90-7.92 (m, 1H), 7.99-8.04 (m, 2H), 8.14-8.16 (m, 2H), 8.64-8.70 (m, 2H), 9.37-9.39 (d, 1H). LC-MS (method 4, gradient 0.02-3.25 min 5-70% B, 3.25-3.70 min 70-95% B, 3.70-4.10 min 95-95% B): Rt = 3.086 min; MS (ESIpos): m/z = 397 [M+H]+. Example I-5 (rac)-N-(1-(3-(Thiazol-2-yl)pyrazin-2-yl)ethyl)-3,5-bis(trifluoromethyl)benzamide
Figure imgf000143_0001
To a solution of (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A,180 mg, 0.26 mmol) in dichloromethane (8 mL) was added 3,5-bis(trifluoromethyl)benzoyl chloride (80 mg, 0.29 mmol), and triethylamine (79 mg, 0.79 mmol). The resulting mixture was stirred at room temperature overnight. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrated. The residue was purified by Prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3.H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 65 B to 95 B in 7 min] to give 38.80 mg (96% purity, 31.9% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.61-1.63 (d, 3H), 6.55-6.59 (m, 1H), 8.03-8.04 (d, 1H), 8.16-8.17 (d, 1H), 8.32 (s, 1H), 8.54 (m, 2H), 8.65-8.66 (d, 1H), 8.69-8.70 (d, 1H), 9.57-9.59 (d, 1H). LC-MS (method 4, gradient 0.01-3.20 min 30-70% B, 3.20-3.50 min 70-95% B, 3.50-4.25 min 95-95% B): Rt = 2.442 min; MS (ESIpos): m/z = 447 [M+H]+.
Example I-6 (rac)-5-(tert-Butyl)-N-(1-(3-(thiazol-2-yl)pyrazin-2-yl)ethyl)nicotinamide
Figure imgf000144_0001
To a solution of 5-tert-butylnicotinic acid (intermediate 7A, 40 mg, 0.22 mmol) in N,N- dimethylformamide (5 mL) was added (rac)-1-(3-(thiazol-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 6A, 46 mg, 0.22 mmol), HATU (127 mg, 0.34 mmol), and N,N-diisopropylethylamine (87 mg, 0.67 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3 .H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 35 B to 80 B in 7 min] to give 17.80 mg (95% purity, 20.6% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.34 (s, 9H), 1.58-1.59 (d, 3H), 6.47-6.53 (m, 1H), 8.00-8.01 (d, 1H), 8.14-8.15 (d, 2H), 8.62-8.63 (d, 1H), 8.67-8.68 (d, 1H), 8.74 (d, 1H), 8.82 (d, 1H), 9.20-9.22 (d, 1H). LC-MS (method 4, gradient 0.01-3.25 min 5-50% B, 3.25-3.80 min 50-95% B, 3.80-4.20 min 95-95% B): Rt = 2.269 min; MS (ESIpos): m/z = 368 [M+H]+.
Example I-7 (rac)-3-Fluoro-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
Figure imgf000145_0001
To a solution of (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 80 mg, 0.40 mmol) in dichloromethane (4 mL) was added 3-fluoro-5-(trifluoromethyl)benzoyl chloride (99 mg, 0.44 mmol), and triethylamine (121 mg, 1.19 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by prep- HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3.H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30 B to 90 B in 7 min] to give 99.20 mg (98% purity, 62.5% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.60-1.62 (d, 3H), 5.59-5.62 (m, 1H), 7.58-7.60 (t, 1H), 7.83-7.88 (t, 2H), 7.95 (s, 1H), 8.69-8.70 (d, 1H), 8.77-8.78 (d, 1H), 8.97-8.98 (d, 2H), 9.16-9.18 (d, 1H). LC-MS (method 4, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.284 min; MS (ESIpos): m/z = 392 [M+H]+.
Example I-8 (rac)-N-(1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethyl)-3,5-bis(trifluoromethyl)benzamide
Figure imgf000146_0001
To a solution of (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 80 mg, 0.40 mmol) in dichloromethane (4 mL) was added 3,5-bis(trifluoromethyl)benzoyl chloride (121 mg, 0.44 mmol), and triethylamine (121 mg, 1.19 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with dichloromethane. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by prep- HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3.H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 32 B to 95 B in 7 min] to give 105.90 mg (98% purity, 59% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.63-1.64 (d, 3H), 5.62-5.65 (m, 1H), 7.57-7.60 (t, 1H), 8.29 (s, 1H), 8.36 (d, 2H), 8.70-8.71 (d, 1H), 8.78-8.79 (d, 1H), 8.96-8.98 (d, 2H), 9.36-9.37 (d, 1H). LC-MS (method 4, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.425 min; MS (ESIpos): m/z = 442 [M+H]+. Example I-9 (rac)-N-(1-(3-(Pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)nicotinamide
Figure imgf000146_0002
To a solution of (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 80 mg, 0.40 mmol) in dichloromethane (4 mL), was added 5-(trifluoromethyl)nicotinoyl chloride (92 mg, 0.44 mmol), and triethylamine (453 mg, 1.19 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with dichloromethane. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by Prep- HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3 .H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 20 B to 70 B in 7 min] to give 98.10 mg (98% purity, 64.6% yield) of the product as an off-white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.61-1.63 (d, 3H), 5.60-5.67 (m, 1H), 7.59-7.61 (t, 1H), 8.46 (m, 1H), 8.70-8.71 (d, 1H), 8.78-8.79 (d, 1H), 8.98-9.00 (d, 2H), 9.09-9.11 (m, 2H), 9.27-9.29 (d, 1H). LC-MS (method 5, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.173 min; MS (ESIpos): m/z = 375 [M+H]+. Example I-10 (rac)-3-Chloro-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)-5-(trifluoromethyl)benzamide
Figure imgf000147_0001
To a solution of (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 80 mg, 0.40 mmol) in dichloromethane (4 mL), was added 3-chloro-5-(trifluoromethyl)benzoyl chloride (106 mg, 0.44 mmol), and triethylamine (121 mg, 1.19 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with dichloromethane. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by Prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3.H2O), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 40 B to 60 B in 7 min] to give 114.2 mg (99% purity, 69.7% yield) of the product as a white solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.60-1.61 (d, 3H), 5.59-5.62 (m, 1H), 7.58-7.60 (t, 1H), 8.01-8.06 (m, 3H), 8.69-8.70 (d, 1H), 8.77-8.78 (d, 1H), 8.96-9.00 (m, 2H), 9.19-9.20 (d, 1H). LC-MS (method 4, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 1.384 min; MS (ESIpos): m/z = 408 [M+H]+. Example I-11 (rac)-5-(tert-Butyl)-N-(1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethyl)nicotinamide
Figure imgf000148_0001
To a solution of 5-tert-butylnicotinic acid (40 mg, 0.22 mmol) in N,N-dimethylformamide (5 mL), was added (rac)-1-(3-(pyrimidin-2-yl)pyrazin-2-yl)ethan-1-amine (intermediate 9A, 45 mg, 0.22 mmol), HATU (127 mg, 0.34 mmol), and N,N-diisopropylethylamine (87 mg, 0.67 mmol). The resulting mixture was stirred at room temperature for 1 h. Water was added and the resulting mixture was extracted with dichloromethane. The combined organic layer was washed with brine and concentrated under vacuum. The residue was purified by Prep-HPLC with the following conditions [Column: Mobile Phase A: Water (10 mmol/L NH4HCO3 + 0.1% NH3.H2O), Mobile Phase B: ACN; Flow rate: 25 mL/min; Gradient: 20 B to 35 B in 7 min] to give 17.70 mg (95% purity, 20.8% yield) of the product as a light yellow solid. 1H-NMR (400 MHz, DMSO-d6): δ [ppm] = 1.29-1.31 (s, 9H), 1.60-1.62 (d, 3H), 5.56-5.63 (m, 1H), 7.55-7.58 (t, 1H), 7.97-7.98 (t, 1H), 8.66-8.72 (m, 3H), 8.77-8.78 (d, 1H), 8.96-8.98 (m, 3H). LC-MS (method 4, gradient 0.01-2.00 min 5-100% B, 2.00-2.70 min 100-100% B): Rt = 0.900 min; MS (ESIpos): m/z = 363 [M+H]+. The following examples were synthesized in analogy to example I-1 starting from intermediate 4A:
Figure imgf000149_0001
Figure imgf000150_0001
Figure imgf000151_0001
Figure imgf000152_0001
Figure imgf000153_0001
Figure imgf000154_0001
Figure imgf000155_0002
Example I-30 (rac)-Methyl 6-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3- carboxylate
Figure imgf000155_0001
(rac) 6-{3-[1-aminoethyl]pyrazin-2-yl}pyridine-3-carboxylate (intermediate 25A, 130 mg, 503 µmol), 3,5-bis(trifluoromethyl)benzoic acid (169 mg, 654 µmol) and DIPEA (260 µl, 1.5 mmol) were dissolved in DMF (3.0 mL). The solution was cooled on an ice-water bath to 0 °C and HATU (287 mg, 755 µmol) was added. The cooling bath was removed and mixture was stirred for 30 min. Then water was added. The precipitated product was collected on a filter funnel, dried under vacuum and eventually purified by preparative HPLC (RP-C18, water-acetonitril gradient with 0.1% TFA). A yield of 260 mg (71% of theory) of the title compound was isolated. LC-MS (method 2): Rt = 2.18 min; MS (ESIpos): m/z = 499 [M+H]+ ¹H-NMR (400 MHz, DMSO-d6) δ [ppm]: -0.008 (1.26), 0.008 (1.63), 1.685 (5.98), 1.702 (6.07), 2.733 (0.41), 2.892 (0.53), 3.363 (0.90), 3.369 (0.69), 3.375 (0.65), 3.381 (0.53), 3.925 (16.00), 5.803 (1.02), 5.820 (1.55), 5.837 (1.02), 8.101 (2.16), 8.103 (2.16), 8.121 (2.48), 8.123 (2.44), 8.259 (2.16), 8.361 (5.21), 8.424 (1.99), 8.429 (1.99), 8.444 (1.75), 8.450 (1.79), 8.695 (3.13), 8.701 (3.83), 8.752 (3.66), 8.758 (3.05), 9.180 (2.04), 9.182 (2.20), 9.186 (2.20), 9.187 (1.99), 9.354 (1.47), 9.371 (1.42). Example I-31 (rac)-6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3-carboxylic acid
Figure imgf000156_0001
(rac)-Methyl 6-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3-carboxylate (example I-30, 185 mg, 371 µmol) was suspended in methanol (3.0 mL) and a previously prepared solution of sodium hydroxide (104 mg, 2.61 mmol) in water (1.0 mL) was added at ambient temperature. The mixture was stirred for 30 min. The reaction mixture was then diluted with water, acidified with 1 M hydrochloric acid and extracted with three portions of ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, evaporated and eventually purified by preparative HPLC (RP-C18, water-acetonitril gradient with 0.1% TFA). A yield of 153 mg (100 % purity, 85 % of theory) of the title compound was isolated. LC-MS (method 2): Rt = 1.84 min; MS (ESIpos): m/z = 485 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.687 (15.76), 1.698 (15.70), 5.823 (0.66), 5.834 (2.72), 5.846 (4.10), 5.857 (2.70), 5.869 (0.62), 8.096 (5.83), 8.110 (6.33), 8.244 (6.75), 8.376 (16.00), 8.413 (4.03), 8.416 (4.25), 8.426 (3.80), 8.430 (4.02), 8.690 (6.82), 8.693 (7.94), 8.743 (7.63), 8.747 (6.99), 9.167 (6.59), 9.169 (6.90), 9.352 (4.20), 9.364 (4.09), 13.492 (0.90).
Example I-32 (rac)-6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methylpyridine-3-carboxamide
Figure imgf000157_0001
(rac)-6-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3-carboxylic acid (70.0 mg, 145 µmol) was dissolved in DMF (2.0 mL). 1-cyclopropyl-N-methylmethanamine hydrogen chloride (26.4 mg, 217 µmol) and DIPEA (130 µl, 720 µmol) were added. The mixture was stirred at ambient temperature for 1 h, then it was charged upon a preparative HPLC device and purified directly (RP-C18 column, water-acetonitril gradient with 0.1% TFA) to yield 67.0 mg (100 % purity, 84 % yield) of the title compound. LC-MS (method 2): Rt = 2.11 min; MS (ESIpos): m/z = 552 [M+H]⁺ ¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: 0.2 (s, 1H), 0.32 (s, 1H), 0.4-0.51 (m, 2H), 0.93-1.12 (m, 1H), 1.68 (d, 3H), 2.95 (m, 2H), 3.11 (m, 3H), 3.39 (m, 1H), 5.92 (m, 1H), 8.02 (m, 2H), 8.25 (s, 1H), 8.40 (s, 2H), 8.68-8.73 (m, 3H)9.38 (d, 1H). Compounds prepared in analogy: I I
Figure imgf000158_0001
I I
Figure imgf000159_0001
Figure imgf000160_0001
I I
Figure imgf000161_0001
Figure imgf000162_0001
I I
Figure imgf000163_0001
I I
Figure imgf000164_0001
I I
Figure imgf000165_0001
Figure imgf000166_0002
Example I-49 (rac)-Methyl 2-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1,3-thiazole-5- carboxylate
Figure imgf000166_0001
(rac)-Methyl 2-{3-[1-aminoethyl]pyrazin-2-yl}-1,3-thiazole-5-carboxylate (intermediate 28A, 300 mg, 1.14 mmol) and DIPEA (400 µL, 2.3 mmol) were dissolved in THF (15.0 mL) and cooled to 0 °C. A solution of 3,5-bis(trifluoromethyl)benzoyl chloride (377 mg, 1.36 mmol) in THF (1.0 mL) was added and stirring was maintained for 30 min. The solvent was distilled, the residue was washed with tert- butylmethyl ether to give 480 mg (84 % yield) of the title compound. LC-MS (method 1): Rt = 1.53 min; MS (ESIpos): m/z = 505 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.107 (1.29), 1.260 (1.91), 1.357 (1.65), 1.615 (7.46), 1.626 (7.32), 1.760 (0.75), 2.422 (0.62), 2.651 (0.56), 3.078 (0.46), 3.602 (0.74), 3.910 (16.00), 6.508 (1.21), 6.520 (1.86), 6.530 (1.24), 8.291 (3.48), 8.438 (1.85), 8.474 (0.78), 8.520 (7.94), 8.697 (8.88), 8.783 (3.57), 8.853 (1.55), 9.542 (1.75), 9.553 (1.77). Example I-50 (rac)-2-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid
Figure imgf000167_0001
(rac)-Methyl 2-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1,3-thiazole-5- carboxylate (example I-49, 570 mg, 1.13 mmol) was suspended in a mixture of methanol (15.0 mL), THF (5.0 mL) and water (5.0 mL). sodium hydroxide (300 µl, 50% in water, 5.7 mmol) was added and the mixture was stirred at 50 °C for 3 h. The solvents were distilled, the residue was diluted with water, acidified with 1M hydrochloric acid and the precipitate was collected by suction and dried under vacuum. Yield: 510 mg (86 % purity, 79 % yield) of the title compound. LC-MS (method 1): Rt = 1.32 min; MS (ESIpos): m/z = 491 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.61 (d, 3H), 6.52 (m, 1H), 8.38 (s, 1H), 8.53 (s, 2H), 8.60 (s, 1H), 8.69 (s, 1H), 8.78 (s, 1H), 9.57 (d, 1H), 13.75 (br s, 1H). Example I-51 (rac)-2-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methyl-1,3-thiazole-5-carboxamide
Figure imgf000168_0001
(rac)-2-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxylic acid (example I-50, 100 mg, 204 µmol) was dissolved in DMF (3.6 mL). 1-cyclopropyl-N- methylmethanamine hydrogen chloride (49.6 mg, 408 µmol) and DIPEA (180 µl, 1.0 mmol) were added and the mixture was stirred at room temperature for 30 min. Then it was directly charged upon a preparative HPLC device and chromatographed (RP C-1810 µm column, water-acetonitrile gradient with 0,1% TFA) to give 39.0 mg (100 % purity, 34 % yield) of the LC-MS (method 2): Rt = 2.31 min; MS (ESIpos): m/z = 558 [M+H]+ ¹H-NMR (500 MHz, DMSO-d6) δ [ppm]: -0.006 (3.66), 0.006 (3.09), 0.116 (0.40), 0.284 (1.32), 0.503 (1.76), 0.511 (5.29), 0.514 (5.29), 0.527 (5.55), 0.539 (1.59), 1.079 (1.50), 1.234 (0.48), 1.617 (15.96), 1.631 (16.00), 2.362 (0.71), 2.636 (0.84), 3.115 (0.75), 3.386 (6.52), 3.400 (6.39), 6.517 (0.66), 6.530 (2.82), 6.544 (4.32), 6.557 (2.78), 6.571 (0.66), 8.309 (6.70), 8.448 (0.66), 8.539 (15.21), 8.675 (8.42), 8.679 (9.12), 8.745 (9.30), 8.749 (8.20), 9.559 (4.28), 9.573 (4.14). By analogy, the following compounds were synthesized: I I
Figure imgf000169_0001
I I
Figure imgf000170_0001
I I
Figure imgf000171_0001
I I
Figure imgf000172_0001
Figure imgf000173_0001
Figure imgf000174_0001
I I
Figure imgf000175_0001
Figure imgf000176_0001
Figure imgf000177_0001
Figure imgf000178_0001
Figure imgf000179_0001
Figure imgf000180_0001
I I
Figure imgf000181_0001
Figure imgf000182_0001
I I
Figure imgf000183_0001
Example I-82 (rac)-N-{1-[3-(5-Cyano-1,3-thiazol-2-yl)pyrazin-2-yl]ethyl}-3,5-bis(trifluoromethyl)benzamide
Figure imgf000184_0001
(rac)-2-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1,3-thiazole-5-carboxamide (example I-62, 75.0 mg, 153 µmol) was dissolved in THF (3.1 mL) Burgess reagent (CAS RN 29684- 56-8, 38.3 mg, 161 µmol;) was added and the mixture was reacted at ambient temperature for 1 h. More Burgess reagent (18.3 mg, 76.6 µmol) was added and stirring was maintained for another 30 min. The mixture was directly charged onto a preparative HPLC device and chromatographed (RP C-1810µm column, water acetonitrile gradient with 0,1%TFA to give 36.0 mg (100 % purity, 50 % yield) of the title compound. LC-MS (method 2): Rt = 2.29 min; MS (ESIpos): m/z = 472 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: -0.022 (0.44), 1.193 (0.46), 1.234 (1.85), 1.611 (15.63), 1.623 (15.64), 2.069 (2.30), 2.423 (0.51), 2.652 (0.43), 3.261 (1.29), 3.910 (0.99), 6.469 (0.68), 6.481 (2.58), 6.492 (3.94), 6.503 (2.58), 8.294 (6.79), 8.522 (16.00), 8.712 (6.84), 8.715 (7.27), 8.823 (7.21), 8.827 (7.00), 8.938 (11.11), 9.557 (3.60), 9.569 (3.49).
Example I-83 (rac)-2-{3-[1-{[3,5-Bis(trifluoromethyl)benzoyl](cyclopropylmethyl)amino}ethyl]pyrazin-2-yl}-N- ethyl-N-methyl-1,3-thiazole-5-carboxamide
Figure imgf000185_0001
(rac)-2-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-ethyl-N-methyl-1,3-thiazole-5- carboxamide (example 72, 196 mg, 369 µmol) was dissolved in DMF (4.0 mL) and sodium hydride (22.1 mg, 60 % in paraffin, 553 µmol) was added. The mixture was stirred at RT for 20 min, then bromomethyl)cyclopropane (110 µl, 1.1 mmol) was added and heated to 60 °C for 3 h. The mixture was directly charged onto a preparative HPLC device and chromatographed (RP C-1810µm column, water acetonitrile gradient with 0,1%TFA to give 66.0 mg (100 % purity, 31 % yield) of the title compound. LC-MS (method 1): Rt = 1.55 min; MS (ESIpos): m/z = 586 [M+H]+ 1H-NMR (600 MHz, DMSO-d6) δ [ppm]: 0.517 (1.85), 1.162 (8.17), 1.688 (6.60), 2.422 (1.07), 2.652 (1.07), 3.480 (6.56), 6.327 (0.76), 7.582 (1.66), 7.835 (1.46), 8.700 (9.40), 8.803 (16.00), 8.807 (13.58). Examples I-84 and I-85 - Separation of enantiomers: 2-(3-{(1R)-1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-ethyl-N-methyl-1,3- thiazole-5-carboxamide and 2-(3-{(1S)-1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)- N-ethyl-N-methyl-1,3-thiazole-5-carboxamide
Figure imgf000185_0002
(rac)-2-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-ethyl-N-methyl-1,3-thiazole-5- carboxamide (example I-72, 400 mg, 0.82 mmol) was submitted to chiral HPLC at 40 °C, using Daicel Chiralpak ID , 5 μm 250*20 mm as stationary phase and a mixture of n-heptane / 2-propanol (1:1) at 18 mL/min as eluent. Two fractions were eluted at 5.16 and 7.09 min, respectively which were freeze-dried to give Example I-84 Yield: 121 mg (30%) eluting at 5.16 min in the preparative HPLC. Analytical chiral HPLC (method 7) Rt = 4.99 min Optical rotation (method 8): [α]D 20 = -88.8° (c = 0.48, CHCl3). Example I-85 Yield: 122 mg (31%) eluting at 7.09 min in the preparative HPLC. Analytical chiral HPLC (method 7) Rt = 6.25 min Optical rotation (method 8): [α]D 20 = 85.5° (c = 0.49, CHCl3). Example I-86 (rac)-Ethyl 1-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1H-pyrazole-4- carboxylate
Figure imgf000186_0001
(rac)-Ethyl 1-{3-[1-aminoethyl]pyrazin-2-yl}-1H-pyrazole-4-carboxylate (intermediate 37A, 330 mg, 1.26 mmol), 3,5-bis(trifluoromethyl)benzoic acid (424 mg, 1.64 mmol) and DIPEA (660 µl, 3.8 mmol) were dissolved in DMF (5.0 mL). The solution was cooled on an ice-water bath to 0 °C and HATU (720 mg, 1.89 mmol) was added. The cooling bath was removed and mixture was stirred for 1 h. Then water was added. The precipitated product was collected on a filter funnel, dried under vacuum. 558 mg (100 % purity, 88 % yield) of the title compound were obtained. LC-MS (method 2): Rt = 2.27 min; MS (ESIpos): m/z = 502 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.291 (7.96), 1.303 (16.00), 1.315 (7.97), 1.637 (12.36), 1.648 (12.24), 2.694 (0.72), 2.737 (1.30), 2.895 (1.44), 4.254 (0.47), 4.263 (1.69), 4.272 (4.12), 4.275 (4.39), 4.284 (4.14), 4.287 (4.18), 4.295 (1.57), 4.299 (1.38), 4.305 (0.43), 5.722 (0.52), 5.734 (2.11), 5.745 (3.17), 5.756 (2.05), 5.768 (0.49), 8.259 (9.18), 8.273 (5.29), 8.448 (12.45), 8.591 (5.52), 8.594 (5.87), 8.803 (5.61), 8.807 (5.64), 8.883 (9.31), 9.436 (3.22), 9.447 (3.13). Example I-87 (rac)-1-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1H-pyrazole-4-carboxylic acid
Figure imgf000187_0001
(rac)-Ethyl 1-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1H-pyrazole-4-carboxylate (example I-86, 555 mg, 1.11 mmol) was suspended in a mixture of THF (4.0 mL), ethanol (4.0 mL) and water (1.0 mL). sodium hydroxide (443 mg, 50 % in water, 5.53 mmol was added and the mixture was heated to 35 °C. Another 80 mg (2.0 mmol) of neat sodium hydroxide were added and stirring was maintained for 30 min at room temperature. The mixture was poured into water, acidified with 4 M hydrochloric acid and the precipitate was collected by suction and eventually dried under vacuum.435 mg (97 % purity, 81 % yield) of the title compound were isolated. LC-MS (method 2): Rt = 1.83 min; MS (ESIpos): m/z = 474 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.177 (0.41), 1.326 (0.41), 1.338 (0.83), 1.498 (0.65), 1.510 (0.61), 1.636 (16.00), 1.648 (15.89), 1.989 (0.77), 5.736 (0.66), 5.748 (2.89), 5.759 (4.09), 5.770 (2.66), 5.782 (0.63), 8.218 (12.06), 8.273 (6.27), 8.461 (14.68), 8.555 (0.59), 8.583 (7.81), 8.586 (8.12), 8.786 (7.92), 8.790 (7.73), 8.831 (12.37), 9.457 (4.05), 9.468 (3.92), 12.750 (2.03). Example I-88 (rac)-1-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N,N-dimethyl-1H-pyrazole- 4-carboxamide
Figure imgf000188_0001
(rac)-1-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-1H-pyrazole-4-carboxylic acid (example I-87,105 mg, 222 µmol), N-methylmethanamine hydrogen chloride (27.1 mg, 333 µmol) and DIPEA (190 µl, 1.1 mmol) were dissolved in DMF (2.0 mL). HATU (143 mg, 377 µmol) was added and the mixture was stirred at room temperature for 1 h. When it was diluted with water, a precipitate formed which was collected by suction and dried under vacuum to give 66.0 mg (98 % purity, 58 % yield) of the title compound. LC-MS (method 2): Rt = 1.89 min; MS (ESIpos): m/z = 501 [M+H]+ ¹H-NMR (600 MHz, DMSO-d6) δ [ppm]: 1.337 (0.63), 1.497 (0.52), 1.509 (0.53), 1.643 (16.00), 1.654 (15.80), 2.734 (1.18), 2.892 (1.45), 2.994 (3.46), 3.168 (3.46), 5.811 (0.70), 5.822 (2.70), 5.834 (4.09), 5.845 (2.63), 5.856 (0.63), 8.141 (11.32), 8.276 (6.41), 8.468 (15.04), 8.556 (0.62), 8.567 (7.42), 8.571 (7.75), 8.739 (11.86), 8.756 (7.64), 8.760 (7.40), 9.445 (4.02), 9.456 (3.90). By analogous procedures, the following example compounds were obtained:
Figure imgf000189_0001
Figure imgf000190_0001
Figure imgf000191_0001
Figure imgf000192_0001
Figure imgf000193_0001
Figure imgf000194_0001
I I
Figure imgf000195_0001
I I
Figure imgf000196_0001
Figure imgf000197_0001
Figure imgf000198_0001
Figure imgf000199_0001
I I
Figure imgf000200_0001
Figure imgf000201_0001
I I
Figure imgf000202_0001
Figure imgf000203_0001
Figure imgf000204_0001
Figure imgf000205_0001
I I
Figure imgf000206_0001
I I
Figure imgf000207_0001
I I
Figure imgf000208_0001
Figure imgf000209_0001
I I
Figure imgf000210_0001
Figure imgf000211_0001
Figure imgf000212_0001
I I
Figure imgf000213_0001
I I
Figure imgf000214_0001
I I
Figure imgf000215_0001
Figure imgf000216_0001
I I
Figure imgf000217_0001
I I
Figure imgf000218_0001
Figure imgf000219_0001
Figure imgf000220_0001
Figure imgf000221_0001
Figure imgf000222_0001
Figure imgf000223_0001
Figure imgf000224_0001
Figure imgf000225_0001
Example I-160 6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N,N-diethylpyridine-3- carboxamide (Enantiomer 1)
Figure imgf000226_0001
To a solution of (rac)-6-{3-[1-Aminoethyl]pyrazin-2-yl}-N,N-diethylpyridine-3-carboxamide (intermediate 50A, 55 mg,0.18 mmol), 3,5-bis(trifluoromethyl)benzoic acid (94 mg, 0.36mmol) in N,N- dimethylformamide (6 mL) was added N,N-diisopropylethylamine (46.5 mg, 0.36 mmol) and HATU (47.5 mg, 0.25 mmol) respectively. After stirring at 25 oC for 2 h, the reaction mixture was purified via prep-HPLC [RP-C18, mobile Phase A: water(0.1% TFA), mobile Phase B: acetonitrile; gradient: 65% B to 75% B in 10 min] to give 70 mg of the mixture of enantiomers as a white solid. The two enantiomers were separated by chiral HPLC [Column: CHIRALPAK IG, 2*25 cm, 5 um; mobile phase A: MTBE (0.5% 2 M ammonia in MeOH), Mobile Phase B: isopropanol; flow rate: 20 mL/min; Gradient: hold 5% B over 10.5 min; 254/220 nm; Rt 1: 5.262 min; Rt 2: 8.757 min] to give the title compound as isomer 1 (24.6 mg (24% yield) as an off-white solid eluting at 5.262 min in chiral prep HPLC). LC-MS (Method 12): Rt = 1.14; MS (ESIpos): m/z 540 [M+H]+. Chiral HPLC (Method 10): Rt = 1.53 min 1H-NMR (400 MHz, DMSO-d6 δ [ppm] 1.05-1.19 (m, 6H), 1.67 (d, 3H), 5.92 (m, 1H), 8.06 (m, 2H), 8.31 (s, 1H), 8.42 (s, 2H), 8.67-8.77 (m, 3H), 9.43 (br s, 1H). Example I-161 6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N,N-diethylpyridine-3- carboxamide (Enantiomer 2)
enantiomer 2 The title compound was obtained from the chiral chromatography described under example I-160 as the second isomer: 20 mg (20% yield) as an off-white solid (eluting at 8.757 min in chiral Prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IG-3, 4.6*50 mm, 3 um; Mobile Phase A: MTBE (0.1% DEA): IPA=95:5, Mobile Phase B: IPA; Flow rate:1 mL/min; Gradient: hold 5% B over 3.5 min] Rt = 1.533 min. Example I-162 6-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyanomethyl)-N- methylpyridine-3-carboxamide (Enantiomer 1)
Figure imgf000227_0001
To a solution of (rac)-6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3- carboxylic acid (example I-31, 80 mg, 0.17 mmol), 2-(methylamino)acetonitrile(18 mg, 0.25 mmol) in N,N-dimethylformamide (6 ml) was added N,N-diisopropylethylamine (107 mg, 0.83 mmol) and HATU (94 mg,0.25 mmol) respectively. After stirring at 25 oC for 2 h, the reaction mixture was purified via prep-HPLC [mobile phase A: water(0.1% TFA), mobile phase B: acetonitrile; gradient: 65% B to 75% B in 10 min] to give 40 mg of the mixture of enantiomers as a white solid. The two enantiomers were separated by Chiral-HPLC [Column: CHIRALPAK IG, 2*25 cm, 5 um; Mobile Phase A: MTBE (0.5% 2 M NH3-MeOH), Mobile Phase B: IPA; Flow rate: 20 mL/min; Gradient: hold 5% B in 8.5 min; 254/220 nm; Rt 1: 4.457 min; Rt 2: 6.687 min] to give the title compound isomer 1 (7.5 mg, 8% yield) as a pink solid (eluting at 4.457 min in chiral Prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IG-3, 4.6*50 mm 3 um; Mobile Phase A: MtBE (0.1% diethylamine): isopropanol 98:2, Mobile Phase B: IPA; Flow rate:1 mL/min; Gradient: 5% B to 5% B in 3 min] Rt = 1.281 min. [a]D 23 = 46 o (c = 0.002, CHCl3). Example I-163 6-(3-{1-[3,5-bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyanomethyl)-N- methylpyridine-3-carboxamide (Enantiomer 2)
Figure imgf000228_0001
The title compound was obtained as the second isomer from the chiral chromatography described under example I-162 (16.9 mg, 19% yield) as a pink solid (eluting at 6.687 min in chiral prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IG-3, 4.6*50 mm 3 um; Mobile Phase A: MtBE (0.1% diethylamine): isopropanol=98:2, Mobile Phase B: isopropanol; flow rate:1 mL/min; gradient: 5% B to 5% B in 3 min] Rt = 1.952 min [a]D23 = -60 o (c = 0.002, CHCl3). LC-MS (Method 12): Rt = 1.08; MS (esiPos): m/z 537 [M+H]+. 1H-NMR (400 MHz, DMSO-d6 δ [ppm]: 1.67 (d, 3H), 3.06 (s, 3H), 4.64 (s, 2H), 5.92 (m, 1H), 8.10 (m, 2H), 8.28 (s, 1H), 8.41 (s, 2H), 8.67-8.77 (m, 3H), 9.46 (m, 1H). Example I-164 6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methylpyridine-3-carboxamide (Enantiomer 1)
ena
Figure imgf000229_0001
To a solution of (rac)-6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3- carboxylic acid (example I-31, 80 mg, 0.17 mmol), cyclopropyl-N-methylmethanamine (28 mg, 0.25 mmol) in N,N-dimethylformamide (6 ml) was added N,N-diisopropylethylamine (107 mg, 0.83 mmol) and HATU (94 mg, 0.25 mmol) respectively. After stirred at 25 oC for 2 h, the reaction mixture was purified via prep-HPLC [Mobile Phase A: Water(0.1%FA), Mobile Phase B: ACN; Gradient: 65% B to 75% B in 10 min] to give 30 mg of the mixture of enantiomers as a pink solid. The two enantiomers were separated by chiral HPLC [Column: CHIRALPAK IC, 2*25 cm, 5 um; mobile phase A: hexane: DCM=3:1 (0.5% 2 M ammonia in MeOH), mobile phase B: isopropanol; flow rate:20 mL/min; gradient: hold 10% B in 22 min; 220/254 nm; Rt 1: 16.225; Rt 2: 19.408] to give the title compound as the frirst eluting isomer (10.7 mg (12% yield) as a pink solid (eluting at 16.225 min in chiral Prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IC, 4.6*50 mm 3 um; Mobile Phase A: (Hexane: DCM=3:1) (0.1% DEA): IPA=90:10, Mobile Phase B: IPA; Flow rate:1 mL/min; Gradient:10% B to 10% B in 7 min] Rt = 4.141 min. Optical rotation: [a]D 23 = 20 o (c = 0.002, CHCl3). LC-MS (Method 12): Rt = 1.17; MS (ESIpos): m/z 552 [M+H]+. 1H-NMR (400 MHz, DMSO-d6 δ [ppm] 0.1-0.7 (m, 4H), 0.81-1.20 (m, 1H), 1.67 (d, 3H), 2.96 (s, 2H), 3.10 (s, 3H), 5.94 (br s, 1H), 8.06 (m, 2H), 8.31 (s, 1H), 8.42 (s, 2H), 8.67-8.77 (m, 3H), 9.43 (br s, 1H). Example I-165 6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)-N-(cyclopropylmethyl)-N- methylpyridine-3-carboxamide (Enantiomer 2)
ena
Figure imgf000230_0001
The title compound was obtained as the second isomer from the chiral chromatography described under example I-164 (7.6 mg, 8% yield) as a pink solid (eluting at 19.408 min in chiral Prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IC, 4.6*50 mm 3 um; Mobile Phase A: (Hexane: DCM=3:1) (0.1% DEA): IPA=90:10, Mobile Phase B: IPA; Flow rate:1 mL/min; Gradient:10% B to 10% B in 7 min] Rt = 5.943 min. Optical rotation: [a]D23 = -32 o (c = 0.002, CHCl3). LC-MS (Method 12): Rt = 1.17; MS (ESIpos): m/z 552 [M+H]+. 1H-NMR (400 MHz, DMSO-d6 δ [ppm] 0.1-0.7 (m, 4H), 0.81-1.20 (m, 1H), 1.67 (d, 3H), 2.96 (s, 2H), 3.10 (s, 3H), 5.94 (br s, 1H), 8.06 (m, 2H), 8.31 (s, 1H), 8.42 (s, 2H), 8.67-8.77 (m, 3H), 9.43 (br s, 1H). Example I-166 N-[1-(3-{5-[(cis)-2,6-Dimethylmorpholine-4-carbonyl]pyridin-2-yl}pyrazin-2-yl)ethyl]-3,5- bis(trifluoromethyl)benzamide (Enantiomer 1) enantiomer
Figure imgf000230_0002
To a solution of (rac)-6-(3-{1-[3,5-Bis(trifluoromethyl)benzamido]ethyl}pyrazin-2-yl)pyridine-3- carboxylic acid (example I-31, 80 mg,0.17 mmol), (cis)-2,6-dimethylmorpholine (28 mg, 0.25 mmol) in N,N-dimethylformamide (6 ml) was added N,N-diisopropylethylamine (107 mg, 0.83 mmol) and HATU (94 mg,0.25 mmol) respectively. After stirred at 25 oC for 2 h, the reaction mixture was purified via prep-HPLC [Mobile Phase A: Water(0.1%FA), Mobile Phase B: ACN; Gradient: 65% B to 75% B in 10 min] to give 67 mg of the mixture of enantiomers as an off-white solid. The two enantiomers were separated by chiral HPLC [Column: CHIRALPAK IG, 2*25 cm, 5 um; mobile phase A: MTBE (0.5% 2 M ammonia in MeOH), mobile phase B: isopropanol; flow rate: 20 mL/min; gradient: hold 5% B in 9 min; 254/220 nm; Rt 1: 4.59 min; Rt 2: 7.081 min] to give the title compound (16.1 mg 16% yield) as an off-white solid (eluting at 4.59 min in chiral prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IG-3, 4.6*50 mm,3.0 um; Mobile Phase A: MTBE (0.1% DEA): IPA = 95:5, Mobile Phase B: IPA; Flow rate:1 mL/min; 5% B to 5% B in 3.5 min] Rt = 1.031 min. Optical rotation: [a]D23 = +103 o (c = 0.003, CHCl3). LC-MS (Method 12): Rt = 1.14; MS (ESIpos): m/z 582 [M+H]+. 1H-NMR (400 MHz, DMSO-d6 δ [ppm] 0.9-1.3 (m, 6H), 1.66 (d, 3H), 2.81-2.95 (m, 1H), 3.40-3.50 (m, 3H), 4.42 (br s, 1H), 5.94 (br s, 1H), 8.06 (m, 2H), 8.31 (s, 1H), 8.42 (s, 2H), 8.67-8.77 (m, 3H), 9.43 (br s, 1H). Example I-167 N-[1-(3-{5-[(cis)-2,6-Dimethylmorpholine-4-carbonyl]pyridin-2-yl}pyrazin-2-yl)ethyl]-3,5- bis(trifluoromethyl)benzamide (Enantiomer 2) enantiomer
Figure imgf000231_0001
The title compound was obtained as the second isomer from the chiral chromatography described under example I-166 (19.5 mg 20% yield) as an off-white solid (eluting at 7.081 min in chiral Prep HPLC). Analytical chiral HPLC [Column: CHIRALPAK IG-3, 4.6*50 mm,3.0 um; Mobile Phase A: MTBE (0.1% DEA): IPA = 95:5, Mobile Phase B: IPA; Flow rate:1 mL/min; 5% B to 5% B in 3.5 min] Rt = 1.324 min. Optical rotation: [a]D 23 = -90 o (c = 0.003, CHCl3). LC-MS (Method 12): Rt = 1.14; MS (ESIpos): m/z 582 [M+H]+. 1H-NMR (400 MHz, DMSO-d6 δ [ppm] 0.9-1.3 (m, 6H), 1.66 (d, 3H), 2.81-2.95 (m, 1H), 3.40-3.50 (m, 3H), 4.42 (br s, 1H), 5.94 (br s, 1H), 8.06 (m, 2H), 8.31 (s, 1H), 8.42 (s, 2H), 8.67-8.77 (m, 3H), 9.43 (br s, 1H).
Figure imgf000232_0001
I I
Figure imgf000233_0001
I I
Figure imgf000234_0001
I I
Figure imgf000235_0001
Figure imgf000236_0001
I I
Figure imgf000237_0001
Figure imgf000238_0001
Figure imgf000239_0001
I I
Figure imgf000240_0001
I I
Figure imgf000241_0001
I I
Figure imgf000242_0001
I I
Figure imgf000243_0001
I
Figure imgf000244_0001
I I
Figure imgf000245_0001
I I
Figure imgf000246_0001
Figure imgf000247_0001
Figure imgf000248_0001
I
Figure imgf000249_0001
Biological Examples Rhipicephalus (Boophilus) microplus – in-vitro contact tests larval cattle tick (Strain Parkhurst, resistant against synthetic pyrethroids) 9 mg compound is solved in 1 mL acetone and diluted with acetone to the desired concentration.250 µL of the test solution is filled in 25 mL glass test tubes and homogeneously distributed on the inner walls by rotation and tilting on a shaking device (2 h at 30 rpm). With a compound concentration of 900 ppm, an inner surface of 44.7 cm2 and a homogeneous distribution, a dose of 5 µg/cm² is achieved. After the solvent has evaporated, each test tube is filled with 20-50 cattle tick larvae (Rhipicephalus microplus), closed with a perforated lid and incubated in a horizontal position at 85 % relative humidity and 27 °C in an incubator. After 48 hours efficacy is determined. The larvae are patted on the ground of the tubes and negative geotactic behaviour is recorded. Larvae that climb back to the top of the vial in a manner comparable to untreated control larvae are marked as alive, larvae not climbing back up comparable to untreated control larvae but are moving uncoordinatedly or only twitching their legs are marked as moribund, tick larvae remaining on the bottom and not moving at all are counted as dead. A compound shows a good efficacy against Rhipicephalus microplus, if at a compound concentration of 5 µg/cm² an efficacy of at least 80 % is monitored. An efficacy of 100 % means all larvae are dead or moribund; 0 % means no larvae are dead or moribund. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 5 µg/cm² (= 500 g/ha): I-5, I-7, I-8, I-9, I-11, I-13, I-20, I-32, I-33, I- 34, I-35, I-37, I-38, I-46, I-59, I-61, I-64, I-65, I-66, I-68, I-69, I-72, I-76, I-82, I-83, I-85, I-88, I-89, I- 90, I-91, I-92, I-93, I-94, I-100, I-113, I-115, I-116, I-118, I-119, I-120, I-124, I-125, I-126, I-127, I-131, I-132, I-133, I-134, I-136, I-137, I-138, I-139. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 5 µg/cm² (= 500 g/ha): I-17, I-24, I-26, I-29, I-51, I-54, I-58, I-75, I- 102, I-103, I-114, I-141, I-143. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 5 µg/cm² (= 500 g/ha): I-6, I-10, I-14, I-15, I-27, I-28, I-128. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 1 µg/cm² (= 100 g/ha): I-1, I-5, I-7, I-8, I-9, I-13, I-20, I-26, I-29, I-32, I-34, I-35, I-37, I-38, I-46, I-58, I-59, I-61, I-64, I-65, I-66, I-68, I-69, I-72, I-76, I-82, I-83, I-85, I-88, I- 89, I-90, I-91, I-92, I-93, I-94, I-100, I-113, I-115, I-118, I-119, I-120, I-124, I-125, I-126, I-127, I-131, I-132, I-133, I-134, I-136, I-137, I-138, I-139, I-141, I-143. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 1 µg/cm² (= 100 g/ha): I-10, I-14, I-24, I-27, I-28, I-33, I-51, I-75, I- 102, I-103, I-114, I-116, I-122, I-128. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 1 µg/cm² (= 100 g/ha): I-6, I-15, I-17. Rhipicephalus (Boophilus) microplus – injection test Solvent: dimethyl sulfoxide To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 mL solvent, and the concentrate is diluted with solvent to the desired concentration. Five adult engorged female ticks (Rhipicephalus microplus) are injected with 1 µL compound solution into the abdomen. The ticks are transferred into replica plates and incubated in a climate chamber. After 7 days egg deposition of fertile eggs is monitored. Eggs where fertility is not visible are stored in a climate chamber till hatching after about 42 days. An efficacy of 100 % means all eggs are infertile; 0 % means all eggs are fertile. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 4 µg/animal: I-2, I-3, I-7, I-8, I-9, I-10, I-17, I-23, I-24, I-56, I-63, I- 64. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 4 µg/animal: I-5, I-13, I-14, I-15, I-20, I-21, I-25, I-53, I-65, I-66. Ctenocephalides felis – in-vitro contact tests adult cat flea 9 mg compound is solved in 1 ml acetone and diluted with acetone to the desired concentration.250 µL of the test solution is filled in 25 mL glass test tubes and homogeneously distributed on the inner walls by rotation and tilting on a shaking device (2 h at 30 rpm). With a compound concentration of 900 ppm, an inner surface of 44.7 cm2 and a homogeneous distribution, a dose of 5 µg/cm² is achieved. After the solvent has evaporated, each test tube is filled with 5-10 adult cat fleas (Ctenocephalides felis), closed with a perforated lid and incubated in a lying position at room temperature and relative humidity. After 48 hours efficacy is determined. The fleas are patted on the ground of the tubes and are incubated on a heating plate at 45-50 °C for at most 5 minutes. Immotile or uncoordinated moving fleas, which are not able to escape the heat by climbing upwards, are marked as dead or moribund. A compound shows a good efficacy against Ctenocephalides felis, if at a compound concentration of 5 µg/cm² an efficacy of at least 80 % is monitored. An efficacy of 100 % means all fleas are dead or moribund; 0 % means no fleas are dead or moribund. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 5 µg/cm² (= 500 g/ha): I-32, I-33, I-35, I-38, I-61, I-64, I-65, I-66, I- 68, I-82, I-83, I-85, I-132, I-133, I-134, I-141. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 5 µg/cm² (= 500 g/ha): I-34, I-118, I-119, I-140. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 5 µg/cm² (= 500 g/ha): I-10, I-19, I-27, I-103. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 1 µg/cm² (= 100 g/ha): I-33, I-61, I-64, I-65, I-66, I-68, I-82, I-83, I-85, I- 132, I-133. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 1 µg/cm² (= 100 g/ha): I-7, I-38. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 1 µg/cm² (= 100 g/ha): I-27, I-34, I-35, I-134. Ctenocephalides felis – oral test Solvent: dimethyl sulfoxide To produce a suitable preparation of active compound, 10 mg of active compound are dissolved in 0.5 mL solvent, and the concentrate is diluted with citrated cattle blood to the desired concentration. Approximately 20 adult unfed cat fleas (Ctenocephalides felis) are placed in a flea chamber whose top and bottom is covered with gauze. A chamber whose bottom is sealed with parafilm, is filled with the blood-compound solution and placed on top of the flea chamber, so that the fleas can suck the blood. The blood chamber is heated to 37 °C whereas the flea chamber is kept at room temperature. After 2 days mortality in % is determined.100 % means all the fleas have been killed; 0 % means none of the fleas have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 ppm: I-7, I-8, I-10, I-12, I-14, I-15, I-16, I-17, I-23, I-24, I-55. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 100 ppm: I-1, I-2, I-3, I-5, I-11, I-13, I-25. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 100 ppm: I-9, I-65. Rhipicephalus sanguineus - in-vitro contact tests with adult brown dog ticks 9 mg compound is solved in 1 mL acetone and diluted with acetone to the desired concentration.250 µL of the test solution is filled in 25 mL glass test tubes and homogeneously distributed on the inner walls by rotation and tilting on a shaking device (2 h at 30 rpm). With a compound concentration of 900 ppm, an inner surface of 44.7 cm2 and a homogeneous distribution, a dose of 5 µg/cm² is achieved. After the solvent has evaporated, each test tube is filled with 5-10 adult brown dog ticks (Rhipicephalus sanguineus), closed with a perforated lid and incubated in a lying position at room temperature and relative humidity. After 48 hours efficacy is determined. The ticks are patted on the ground of the tubes and are incubated on a heating plate at 45-50 °C for at most 5 minutes. Immotile or uncoordinated moving ticks, which are not able to escape the heat by climbing upwards, are marked as dead or moribund. A compound shows a good efficacy against Rhipicephalus sanguineus, if at a compound concentration of 5 µg/cm² an efficacy of at least 80 % is monitored. An efficacy of 100 % means all ticks are dead or moribund; 0 % means no ticks are dead or moribund. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 5 µg/cm² (= 500 g/ha): I-2, I-7, I-59, I-64, I-68, I-85, I-132, I-133, I-134, I- 138. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 5 µg/cm² (= 500 g/ha): I-9, I-10, I-16, I-34, I-48, I-54, I-65, I-66, I-72, I-83, I- 93, I-94, I-103, I-131. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 1 µg/cm² (= 100 g/ha): I-132, I-133, I-134, I-138. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 1 µg/cm² (= 100 g/ha): I-131, I-132. Meloidogyne incognita - test Solvent: 125.0 parts by weight of acetone To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water to the desired concentration. Vessels are filled with sand, a solution of the active ingredient, a suspension containing eggs and larvae of the southern root-knot nematode (Meloidogyne incognita) and salad seeds. The salad seeds germinate and the seedlings grow. Galls develop in the roots. After 14 days the nematicidal activity is determined based on the percentage of gall formation.100 % means no galls were found and 0 % means the number of galls found on the roots of the treated plants was equal to that in untreated control plants. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 20 ppm: I-55, I-82. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 20 ppm: I-17, I-52, I-54, I-63. Diabrotica balteata – spray test Solvent: 78.0 parts by weight of acetone 1.5 parts by weight of dimethylformamide Emulsifier: alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Soaked wheat seeds (Triticum aestivum) are placed in a multiple well plate filled with agar and some water and are incubated for 1 day to germinate (5 seeds per well). The germinated wheat seeds are sprayed with a test solution containing the desired concentration of the active ingredient. Afterwards each unit is infected with 10-20 larvae of the banded cucumber beetle (Diabrotica balteata). After 7 days efficacy in % is determined. 100 % means all the seedlings have grown up like in the untreated, uninfected control; 0 % means none of the seedlings have grown. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 g/ha (= 32 µg/well): I-1, I-3, I-10, I-12, I-15, I-16, I-17, I-18, I-19, I-20, I-21, I-22, I-24, I-25, I-26, I-27, I-29, I-36, I-39, I-40, I-44, I-45, I-46, I-48, I-51, I-52, I-53, I-54, I- 56, I-59, I-63, I-66, I-67, I-68, I-69, I-70, I-71, I-72, I-75, I-76, I-77, I-82, I-83, I-85, I-88, I-89, I-90, I-92, I-93, I-94, I-96, I-97, I-98, I-100, I-102, I-103, I-104, I-105, I-106, I-112, I-113, I-114, I-115, I-116, I-118, I-119, I-120, I-121, I-124, I-126, I-131, I-132, I-133, I-134, I-138, I-141, I-142, I-143, I-152, I-155. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 100 g/ha (= 32 µg/well): I-5, I-13, I-14, I-28, I-34, I-43, I-139. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 20 g/ha (= 6.4 µg/well): I-8, I-10, I-12, I-13, I-17, I-19, I-21, I-22, I-24, I-25, I-26, I-28, I-29, I-41, I-51, I-52, I-56, I-63, I-66, I-69, I-71, I-72, I-76, I-83, I-85, I-88, I-89, I-92, I- 93, I-96, I-98, I-100, I-102, I-103, I-104, I-106, I-113, I-115, I-116, I-118, I-119, I-124, I-131, I-132, I- 133, I-134, I-143, I-152, I-155. In this test, for example, the following compounds from the preparation examples showed good activity of 80 % at an application rate of 20 g/ha (= 6.4 µg/well): I-3, I-14, I-20, I-48, I-53, I-57. Myzus persicae – oral test Solvent: 100 parts by weight acetone To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water to the desired concentration. 50 µL compound solution is filled in microtiter plates and 150 µL IPL41 insect medium (33 % + 15 % sugar) is added to obtain a total volume of 200 µL per well. Afterwards the plates are sealed with parafilm through which a mixed population of the green peach aphid (Myzus persicae) can suck on the compound preparation. After 5 days mortality in % is determined.100 % means all aphids have been killed and 0 % means none of the aphids have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 4 ppm: I-34. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 4 ppm: I-20. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 0.8 ppm: I-8. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 0.8 ppm: I-10. Myzus persicae – spray test Solvent: 78.0 parts by weight acetone 1.5 parts by weight dimethylformamide Emulsifier: alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvents and is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Chinese cabbage (Brassica pekinensis) leaf disks infected with all instars of the green peach aphid (Myzus persicae), are sprayed with a preparation of the active ingredient of the desired concentration. After 5 days mortality in % is determined.100 % means all aphids have been killed and 0 % means none of the aphids have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 g/ha: I-8, I-10. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 100 g/ha: I-28, I-38, I-84, I-85, I-88, I-160, I-164, I-166. Nezara viridula – spray test Solvent: 78.0 parts by weight of acetone 1.5 parts by weight of dimethylformamide Emulsifier: alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, and the concentrate is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Barley plants (Hordeum vulgare) infested with larvae of the southern green stink bug (Nezara viridula) are sprayed with a test solution containing the desired concentration of the active ingredient. After 4 days mortality in % is determined.100 % means all the stink bugs have been killed; 0 % means none of the stink bugs have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 500 g/ha: I-83, I-93, I-99, I-131, I-132, I-133, I-134, I-139, I-141, I- 155. In this test, for example, the following compounds from the preparation examples showed good activity of 90 % at an application rate of 100 g/ha: I-9. Nilaparvata lugens – spray test Solvent: 78.0 parts by weight of acetone 1.5 parts by weight of dimethylformamide Emulsifier: alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvents and is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Rice plants (Oryza sativa) are sprayed with a preparation of the active ingredient of the desired concentration and the plants are infested with the brown planthopper (Nilaparvata lugens). After 4 days mortality in % is determined.100 % means all planthoppers have been killed and 0 % means none of the planthoppers have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 500 g/ha: I-83, I-85, I-132, I-134, I-140, I-141. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 g/ha: I-8. Spodoptera frugiperda – spray test Solvent: 78.0 parts by weight acetone 1.5 parts by weight dimethylformamide Emulsifier: alkylarylpolyglycol ether To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvents and is diluted with water, containing an emulsifier concentration of 1000 ppm, to the desired concentration. Further test concentrations are prepared by dilution with emulsifier containing water. Maize (Zea mays) leaf sections are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf sections are infested with fall armyworm larvae (Spodoptera frugiperda). After 7 days mortality in % is determined.100 % means all caterpillars have been killed and 0 % means none of the caterpillars have been killed. In this test, for example, the following compounds from the preparation examples showed good activity of 100 % at an application rate of 100 g/ha: I-1, I-8, I-10, I-13, I-19, I-20, I-21, I-22, I-23, I-24, I-25, I- 32, I-36, I-38, I-39, I-45, I-46, I-47, I-48, I-51, I-56, I-58, I-63, I-65, I-66, I-67, I-69, I-72, I-73, I-75, I- 76, I-77, I-83, I-85, I-88, I-89, I-90, I-92, I-93, I-94, I-98, I-100, I-101, I-102, I-103, I-105, I-106, I-113, I-114, I-115, I-116, I-118, I-119, I-120, I-122, I-124, I-125, I-128, I-131, I-132, I-133, I-134, I-136, I- 137, I-138, I-139, I-140, I-141, I-142, I-143, I-148, I-151, I-152, I-155, I-157, I-159, I-160, I-164, I-166. In this test, for example, the following compounds from the preparation examples showed good activity of 83 % at an application rate of 100 g/ha: I-12, I-17, I-41, I-59, I-60. Aedes aegypti test (AEDSAE surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME) In order to produce a sufficient, active ingredient containing solution it is necessary to solve the test compound in the solvent-mix (acetone at 2 mg/ml / RME 2000 ppm). This solution is pipetted onto a glazed tile and after evaporation of the acetone, adult mosquitoes of the species Aedes aegypti strain MONHEIM are placed onto the dried surface. The exposure time is 30 minutes. Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died. The following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m2: I-7, I-8, I-9, I-10, I-85. The following examples showed in this test efficacy of 80-100% at a surface concentration of 4 mg/m2: I- 7, I-8, I-9, I-10. Anopheles funestus test (ANPHFU surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME) In order to produce a sufficient, active ingredient containing solution it is necessary to solve the test compound in the solvent-mix (acetone at 2 mg/ml / RME 2000 ppm). This solution is pipetted onto a glazed tile and after evaporation of the acetone, adult mosquitoes of the species Anopheles funestus strain FUMOZ-R (Hunt et al., Med. Vet. Entomol.2005 Sep; 19(3): 271-275) are placed onto the dried surface. The exposure time is 30 minutes. Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died. The following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m2: I-7, I-8, I-9, I-10, I-85. The following examples showed in this test efficacy of 80-100% at a surface concentration of 4 mg/m2: I- 9. Musca domestica test (MUSCDO surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME) In order to produce a sufficient, active ingredient containing solution it is necessary to solve the test compound in the solvent-mix (acetone at 2 mg/ml / RME 2000 ppm). This solution is pipetted onto a glazed tile and after evaporation of the acetone, adult flies of the species Musca domestica strain WHO- N are placed onto the dried surface. The exposure time is 30 minutes. Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died. The following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m2: I-8, I-10, I-85. The following examples showed in this test efficacy of 80-100% at a surface concentration of 4 mg/m2: I- 7, I-8. Blattella germanica test (BLTTGE surface treatment & contact assay) Solvent: Aceton + 2000 ppm rapeseed oil methyl ester (RME) In order to produce a sufficient, active ingredient containing solution it is necessary to solve the test compound in the solvent-mix (acetone at 2 mg/ml / RME 2000 ppm). This solution is pipetted onto a glazed tile and after evaporation of the acetone, adult animals of the species Blattella germanica strain PAULINIA are placed onto the dried surface. The exposure time is 30 minutes. Mortality in percent (%) is determined 24 hours after contact of the insects to the treated surface. 100% mortality means that all tested insects are dead, whereas 0% means that no insect died. The following examples showed in this test efficacy of 80-100% at a surface concentration of 20 mg/m2: I-7, I-8, I-10.

Claims

Claims: 1. Compounds of the general formula (I)
Figure imgf000261_0001
in which R1 is hydrogen; in each case optionally substituted C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C2-C6haloalkynyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl; or heterocyclyl-C1-C6alkyl, wherein the heterocyclyl is selected from the group consisting of saturated and partially unsaturated 3- to 10-membered heterocyclyl, 5-membered heteroaryl, 6-membered heteroaryl, 9-membered heteroaryl and 10-membered heteroaryl and the heterocyclyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3halo- alkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl R2 is phenyl or a 5- or 6-membered heteroaryl, each of which is optionally substituted with 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C6haloalkyl, C1-C6alkoxy, C3-C6cycloalkoxy, C1-C6haloalkoxy, hydroxy-C1-C6alkyl, -CO2C1-C6alkyl, -NH(C1-C6alkyl), -N(C1-C6alkyl)2, S-C1- C6alkylsulfinimidoyl, S-C3-C6cycloalkylsulfinimidoyl, S-C2-C6alkenylsulfinimidoyl, S- C2-C6alkinylsulfinimidoyl, S-phenylsulfinimidoyl, S-heterocyclylsulfinimidoyl, S- heteroarylsulfinimidoyl, S-C1-C6alkylsulfonimidoyl, S-C3-C6cycloalkylsulfonimidoyl, S-C2-C6alkenylsulfonimidoyl, S-C2-C6alkinylsulfonimidoyl, S-phenylsulfonimidoyl, S- heterocyclylsulfonimidoyl, S-heteroarylsulfonimidoyl, -C(=NOC1-C6alkyl)H, - C(=NOC1-C6alkyl)-C1-C6alkyl, (C1-C6alkyl)3-silyl; - and the substructures S1 – S9, in which the bond to the phenyl or 5- or 6-membered heteroaryl is marked with a # and Z is CO or CS and Y is independently selected from CO or SO2;
Figure imgf000262_0001
R21 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, C3-C6cycloalkyl, -C1-C6alkyl-C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; R22 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, -C1-C6alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R23 is independently selected from in each case optionally substituted C1- C6alkyl, C1-C6haloalkyl, C3-C6cycloalkyl and phenyl; R24 is in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C6haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; or R21 and R22 together with the nitrogen atom to which they are attached, represent a monocyclic or polycyclic optionally substituted 3- to 12-membered saturated or unsaturated heterocyclyl which may contain further heteroatoms; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycanocycloalkyl, C3-C6halocycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C6cyanocycloalkyl, C1- C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R3 is hydrogen or C1-C6alkyl optionally substituted with 1 to 3 substituents selected from halogen, C3-C6-cycloalkyl and C1-C6-alkoxy; R4 is a monocyclic heterocycle selected from the group consisting of a 5-membered heteroaryl, a 6-membered heteroaryl and a 3-6 membered heterocyclyl, each of which containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, and each of which is optionally substituted by 1, 2, 3 or 4 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C6alkyl-C3-C6cycloalkyl, C1-C6haloalkyl, C3-C6halocycloalkyl, C1- C6alkoxy, C3-C6cycloalkoxy, C1-C6haloalkoxy, hydroxy-C1-C6alkyl, -NH(C1-C6alkyl), - NH(C1-C6alkyl-C3-C6cycloalkyl), -N(C1-C6alkyl)2, -N(C1-C6alkyl)(C1-C6alkyl-C3- C6cycloalkyl), -CO2C1-C6alkyl, S-C1-C6alkylsulfinimidoyl, S-C3- C6cycloalkylsulfinimidoyl, S-C2-C6alkenylsulfinimidoyl, S-C2-C6alkinylsulfinimidoyl, S-phenylsulfinimidoyl, S-heterocyclylsulfinimidoyl, S-heteroarylsulfinimidoyl, S-C1- C6alkylsulfonimidoyl, S-C3-C6cycloalkylsulfonimidoyl, S-C2-C6alkenylsulfonimidoyl, S-C2-C6alkinylsulfonimidoyl, S-phenylsulfonimidoyl, S-heterocyclylsulfonimidoyl, S- heteroarylsulfonimidoyl, -C(=NOC1-C6alkyl)H, -C(=NOC1-C6alkyl)-C1-C6alkyl; - and 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1- C6alkyl, C3-C6cycloalkyl, C3-C6cycanocycloalkyl, C3-C6halocycloalkyl, C3- C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1- C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; - and the following substructures S10 – S18, in which the bond to the pyrazine is marked with a # and Z is CO or CS and Y is independently selected from CO or SO2:
Figure imgf000265_0001
R41 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl, C3-C6cycloalkyl, -C1-C6alkyl-C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; R42 is hydrogen or in each case optionally substituted C1-C6alkyl, C1- C6haloalkyl and C3-C6cycloalkyl; R43 is independently selected from in each case optionally substituted C1- C6alkyl, C1-C6haloalkyl, C3-C6cycloalkyl and phenyl; R44 is in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C6haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and heterocyclyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a monocyclic or polycyclic optionally substituted 3- to 12-membered saturated or unsaturated heterocyclyl which may contain further heteroatoms; R5 is hydrogen, halogen, -CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C1-C3cyanoalkyl, C3-C4-cycloalkyl, C3-C4halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1- C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, -NH2, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3alkylthio, C1-C3alkylsulfinyl, C1- C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl; R6 is hydrogen, halogen, -CN, or in each case optionally substituted C1-C3-alkyl, C1-C3- haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, -CO2(C1- C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), -CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1-C4alkyl)H, or -C(=NOC1- C4alkyl)-C1-C4alkyl, -NH2, -NH(C1-C3alkyl), -N(C1-C3alkyl)2, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylthio, C3-C6cycloalkylsulfinyl, C3- C6cycloalkylsulfonyl; and salts and N-oxides thereof. 2. The compounds according to claim 1, in which R1 is hydrogen; or in each case optionally substituted C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C1-C6alkoxyC1-C6alkyl, C1-C6alkylthioC1-C6alkyl, C1- C6alkylsulfinylC1-C6alkyl, C1-C6alkylsulfonylC1-C6alkyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C6alkyl; or phenyl-C1-C6alkyl, in which phenyl is optionally substituted with 1 to 5 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cyano- cycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1- C3cyanoalkylsulfonyl; or heterocyclyl-C1-C3alkyl, wherein the heterocyclyl is selected from the group consisting of tetrahydropyranyl, tetrahydrofuranyl, oxetanyl and azetidinyl, or heteroaryl, wherein the heteroaryl is selected from the group consisting of pyridyl, pyrimidinyl, pyrazyl, pyridazinyl, thiophenyl, furanyl, pyrazolyl, imidazolyl, triazolyl, thiazolyl, and oxazolyl, and wherein the heteroaryl or the heterocyclyl is optionally substituted with 1 to 3 substituents, each independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cycanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1-C3halo- alkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; R2 is selected from the group consisting of phenyl, pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole and thiophene, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C4alkoxy, C3-C6cycloalkoxy, C1-C3haloalkoxy, hydroxy-C1-C4alkyl, -CO2C1-C4alkyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -C(=NOC1- C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl and (C1-C4alkyl)3-silyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; - and the substructures S1, S4, S7, S8 and S9, in which the bond to the aforementioned phenyl, pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole or thiophene is marked with a # and Z is CO or CS; -
Figure imgf000267_0001
R21 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, C3-C6cycloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and 3- to 6-membered heterocyclyl; R22 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R24 is in each case optionally substituted C1-C4alkyl, C2-C6alkenyl, C2- C6alkynyl, C1-C4haloalkyl, C3-C6cycloalkyl, phenyl, heteroaryl and 3- to 6-membered heterocyclyl; wherein the aforementioned optionally substituted radicals in the definitions of R21, R22 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1- C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; or R21 and R22 together with the nitrogen atom to which they are attached, represent a 4- to 12-membered saturated or unsaturated heterocyclyl which may contain up to two further heteroatoms selected from the group of oxygen, nitrogen and sulfur and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, -SF5, and -NH2; and C1-C4alkyl, C3-C6cycloalkyl, C1-C4haloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C4alkylthio, C1-C4alkylsulfinyl, C1-C4alkylsulfonyl, C3- C6cycloalkylsulfanyl, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1- C4haloalkylthio, C1-C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl; R3 is hydrogen or C1-C6alkyl optionally substituted with halogen, cyano, C3-C6cycloalkyl or C1- C4alkoxy; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine, and thiazole, pyrazole, pyrrole, oxazole, isothiazole, isoxazole, thiophene and imidazole, each of which is optionally substituted by 1, 2 or 3 substituents independently selected from the group consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, C1-C4alkoxy, C3-C6cycloalkoxy, C1-C3haloalkoxy, hydroxy-C1-C4alkyl, -CO2C1-C4alkyl, -NH(C1-C4alkyl), -N(C1-C4alkyl)2, -C(=NOC1- C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl and (C1-C4alkyl)3-silyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C3alkylsulfonyl, C3- C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; - and the substructures S10, S11, S13, S14, S16, S17 and S18, in which the bond to the aforementioned pyridine, pyrimidine, pyrazine, pyridazine, thiazole, pyrazole, pyrrole, oxazole, isothiazole, isoxazole, thiophene or imidazole is marked with a # and Z is CO or CS;
Figure imgf000269_0001
R41 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, C3-C6cycloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and 3- to 6-membered heterocyclyl; R42 is hydrogen or in each case optionally substituted C1-C4alkyl, C1- C4haloalkyl, -C1-C4alkyl-C3-C6cycloalkyl and C3-C6cycloalkyl; R43 is independently selected from in each case optionally substituted C1- C4alkyl, C1-C4haloalkyl and C3-C6cycloalkyl; R44 is in each case optionally substituted C1-C4alkyl, C1-C4haloalkyl, C3- C6cycloalkyl, phenyl, heteroaryl and 3- to 6-membered heterocyclyl; wherein the aforementioned optionally substituted radicals in the definitions of R41, R42, R43 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1- C4haloalkoxy, C1-C3alkylsulfonyl, C3-C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a 4- to 12-membered saturated or unsaturated heterocyclyl which may contain up to two further heteroatoms selected from the group of oxygen, nitrogen, sulfur and silicon and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, -SF5, and -NH2; and C1-C4alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C4alkoxy-C1-C6alkyl, C1-C4alkylthio, C1- C4alkylsulfinyl, C1-C4alkylsulfonyl, C3-C6cycloalkylsulfanyl, C3- C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1-C4haloalkylthio, C1- C4haloalkylsulfinyl, C1-C4haloalkylsulfonyl; - and 3- to 6-membered heterocyclyl or a 5- to 6-membered heteroaryl each containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6- membered heterocyclyl or the 5- to 6-membered heteroaryl substituent may optionally carry 1,
2 or 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3-C6cycloalkyl-C1-C6alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl; R5 is hydrogen, halogen, -CN, NH2, or in each case optionally substituted C1-C3-alkyl, C3-C4- cycloalkyl, C1-C3alkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), - CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1- C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3- alkylthio, C3-C6cycloalkylthio, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C3alkyl; R6 is hydrogen, halogen, -CN, NH2, or in each case optionally substituted C1-C3-alkyl, C3-C4- cycloalkyl, C1-C3alkoxy, -CO2(C1-C3alkyl), -CH-(C1-C3alkoxy)2, -CONH(C1-C4alkyl), - CON(C1-C4alkyl)2, -NHCO-C1-C4alkyl, -N(C1-C4alkyl)CO-C1-C4alkyl, -C(=NOC1- C4alkyl)H, or -C(=NOC1-C4alkyl)-C1-C4alkyl, NH(C1-C3alkyl), N(C1-C3alkyl)2, C1-C3- alkylthio, C3-C6cycloalkylthio, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2 and C1-C3alkyl; and salts and N-oxides thereof.
3. The compounds according to claim 1 or 2, in which R1 is hydrogen; or C1-C6alkyl, C3-C6cycloalkylC1-C6alkyl, C2-C6alkenyl, C2-C6haloalkenyl, C2- C6alkynyl, C2-C6haloalkynyl, C1-C3alkoxyC1-C3alkyl, C1-C3alkylthioC1-C3alkyl, C1- C3alkylsulfinylC1-C3alkyl, C1-C3alkylsulfonylC1-C3alkyl, C1-C6haloalkyl, C1-C6cyanoalkyl; R2 is selected from the group consisting of pyrazole, phenyl, pyridine, pyrimidine, pyrazine, and pyridazine, each of which is optionally substituted by a total of 1, 2 or 3 substituents, wherein 1, 2 or 3 of the optional substituents are independently selected from group A consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C4alkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3-C4cycloalkyl, C3- C4halocycloalkyl, C3-C4cyanocycloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, C3- C4cycloalkoxy, C1-C3cyanoalkoxy, -CO2C1-C4alkyl and (C1-C3alkyl)3-silyl; and optionally 1 of the optional substituents may be selected from group B consisting of - the substructures S1, S4, S7, S8 and S9, in which the bond to the phenyl, pyridine, pyrimidine, pyrazine, or pyridazine is marked with a # and Z is CO;
Figure imgf000272_0001
R21 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl; R22 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl and C3-C4cycloalkyl; R24 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl and phenyl; wherein the aforementioned optionally substituted radicals in the definitions of R21, R22 and R24 are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1- C3haloalkyl; R3 is hydrogen or C1-C6alkyl; R4 is selected from the group consisting of pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene and imidazole, wherein the aforementioned 6-membered heteroaryl are each optionally substituted by 1, 2 or 3 substituents and the aforementioned 5-membered heteroaryl are each optionally substituted by 1 or 2 substituents, wherein in each case up to all of the optional substituents are independently selected from group D consisting of - halogen, hydroxy, -CN, -COOH, -NO2, -NH2, -SF5; - and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3cyanoalkyl, C3- C4cyanocycloalkyl, C1-C3alkoxy, C3-C4cycloalkoxy, C1-C3haloalkoxy, C1- C3cyanoalkoxy, hydroxy-C1-C3alkyl, -CO2C1-C3alkyl, -NH(C1-C3alkyl), -N(C1- C3alkyl)2, -C(=NOC1-C3alkyl)H, -C(=NOC1-C3alkyl)-C1-C3alkyl and (C1-C3alkyl)3- silyl; and optionally 1 of the optional substituents may be selected from group E consisting of - the substructures S10, S13, S16, S17 and S18, in which the bond to the aforementioned pyridine, pyrimidine, pyrazine, pyridazine, pyrazole, pyrrole, thiazole, oxazole, isothiazole, isoxazole, thiophene or imidazole is marked with a # and Z is CO;
Figure imgf000273_0001
R41 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, C3-C4cycloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and 3- to 6-membered heterocyclyl containing 1 heteroatoms selected from the group consisting of N, O, and S; R42 is hydrogen or in each case optionally substituted C1-C3alkyl, C1- C3haloalkyl, -C1-C2alkyl-C3-C4cycloalkyl and C3-C4cycloalkyl; R44 is in each case optionally substituted C1-C3alkyl, C1-C3haloalkyl, C3- C4cycloalkyl; wherein the aforementioned optionally substituted radicals defined for R41, R42 and R44 are optionally substituted with up to 2 substituents independently selected from the group consisting of halogen, -CN, -NO2, -Si(CH3)3, C1-C3alkyl, C1-C3haloalkyl; or R41 and R42 together with the nitrogen atom to which they are attached, represent a monocyclic 4- to 8-membered saturated heterocyclyl which may contain up to one further heteroatom selected from the group of oxygen, nitrogen, sulfur and silicon and which is optionally substituted with one to three substituents selected from the group consisting of halogen, =O (oxo), =S (thiono), hydroxy, -CN, -NO2, and -NH2; and C1-C3alkyl, C3-C4cycloalkyl, C1-C3haloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R5 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4-cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; R6 is hydrogen, halogen, -CN, C1-C3-alkyl, C1-C3-haloalkyl, C3-C4cycloalkyl, C1-C3alkoxy, C1- C3haloalkoxy; and salts and N-oxides thereof.
4. The compounds according to claim 1, 2 or 3, in which R1 is hydrogen; methyl, ethyl, n-propyl, isopropyl, cyanomethyl, cyclopropylmethyl, methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methylthioethyl, ethylthioethyl, methylsulfonylethyl, ethylsulfonylethyl; R2 is selected from the group consisting of pyrazole, phenyl and pyridine each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxy, -CN, -COOH, -CONH2, -NO2, -NH2, -SF5, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, cyclopropyl, cyclobutyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, 1-cyano-1-methyleth-1-yl,, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, (CH3)3-silyl; phenylsulfonyl which may carry a fluorine, chlorine or methyl substituent; R3 is hydrogen, methyl, ethyl, n-propyl, or isopropyl; R4 is selected from the group consisting of pyridin-2-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H- pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, -COOH, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, cyclobutyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, cyanomethoxy, methylthio, methylsulfinyl, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, difluoromethylthio, trifluoromethylthio, difluoromethylsulfinyl, trifluoromethylsulfinyl, difluoromethylsulfonyl, trifluoromethylsulfonyl, -COOCH3, - COOCH2CH3, and the substructures S13, in which the bond to the aforementioned pyridin-2-yl, pyrimidin- 2-yl, pyrimidin-4-yl, pyrazin-3-yl, and 1,3-thiazol-2-yl, 1,3-oxazol-2-yl, 1,2-oxazol-3-yl, 1,2-thiazol-3-yl, 1H-pyrazol-1-yl, 1H-pyrazol-3-yl, 1H-imidazol-4-yl, is marked with a # and Z is CO;
Figure imgf000275_0001
R41 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R42 is hydrogen, methyl, ethyl, n-propyl, propane-2-yl, butane-2-yl, 2,2,2- trifluoroethyl, 2-trifluoromethoxyethyl, cyanomethyl, cyclopropyl, cyclopropyl- methyl, or 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, azepane, morpholine, oxazepane, azasilolidine, azasilinane, azasilepane each of which is optionally substituted with 1 or 2 methyl groups; R5 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; R6 is hydrogen, fluorine, chlorine, bromine, iodine, -CN, methyl, ethyl, n-propyl, isopropyl, butyl, tert-butyl, difluoromethyl, trifluoromethyl, pentafluoroethyl, cyanomethyl, cyclopropyl, cyclobutyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy or cyanomethoxy; and salts and N-oxides thereof.
5. The compounds according to claim 1, 2, 3 or 4, in which R1 is hydrogen, or cyclopropylmethyl; R2 is selected from the group consisting of pyrazol, phenyl and pyridine, each of which is optionally substituted by 1 or 2 substituents independently selected from the group consisting of fluorine, chlorine, bromine, iodine, -CN, -SF5, methyl, ethyl, n-propyl, isopropyl, tert- butyl, 1-cyano-1-methyleth-1-yl, cyclopropyl, 1-cyanocyclopropyl, difluoromethyl, trifluoromethyl, methoxy, ethoxy, difluoromethoxy, difluoromethoxy, trifluoromethoxy, methylsulfonyl, ethylsulfonyl, cyclopropylsulfonyl, trifluoromethylsulfonyl, 4-fluoro- phenylsulfonyl, difluoromethylsulfonyl; R3 is methyl; R4 is selected from the group consisting of pyridine-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl, 1H- pyrazol-1-yl each of which is optionally substituted by 1 substituent selected from the group consisting of fluorine, chlorine, bromine, -CN, methyl, ethyl, trifluoromethyl, methoxy, ethoxy, -COOH, -COOCH3, -COOCH2CH3, and the substructure S13, in which the bond marked with # is connected to the C-5-position of the aforementioned pyridin-2-yl, pyrimidin-2-yl, 1,3-thiazol-2-yl -, or to the C-4-position in the above mentioned 1H-pyrazol- 1-yl, and Z is CO;
Figure imgf000277_0001
R41 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl, cyclopropyl; R42 is hydrogen, methyl, ethyl, propane-2-yl, 2,2,2-trifluoroethyl, cyanomethyl, cyclopropylmethyl, 2-methyl-n-propyl; R41 and R42 together with the nitrogen atom to which they are attached, represent pyrrolidine, piperidine, morpholine, 2,6-dimethylmorpholine, oxazepane, or (Si,Si- dimethyl)azasilinane; R5 is hydrogen or methyl; R6 is hydrogen or methyl; and salts and N-oxides thereof.
6. The compounds according to any one of claims 1 to 5, in which R2 is selected from the group consisting of phenyl, pyridyl, thiophene, pyrazole and imidazole,which may be substituted as defined in any of the preceding claims; and salts and N-oxides thereof.
7. The compounds according to any one of claims 1 to 6, in which R4 is selected from the group consisting of pyridine, pyrimidine pyrazine, pyridazine, each of which may be substituted as defined in any of the preceding claims; and salts and N-oxides thereof.
8. The compounds according to any one of claims 1 to 6, in which R4 is selected from the group consisting of each of thiazole, pyrazole, pyrrole, oxazole, isothiazole, isoxazole, thiophene and imidazole, preferably thiazole, pyrazole, isothiazole and imidazole, more preferably thiazole, pyrazole each of which may be substituted as defined in any of the preceding claims; and salts and N-oxides thereof.
9. The compounds according to any of the preceding claims wherein R2 is the substructure Q1 in which the bond to the C=O-group is marked with a #:
Figure imgf000278_0001
wherein R25 is hydroxy, -NH2, -SO2NH2, C4-C6alkyl, C4alkoxy, C1-C3cyanoalkyl, C3-C6cycloalkyl, C3- C6halocycloalkyl, C3-C6cyanocycloalkyl, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C3-C6cycloalkylsulfanyl, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C1- C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C1-C3cyanoalkoxy, hydroxy-C1-C4alkyl, -NH(C1- C4alkyl), -N(C1-C4alkyl)2, -NHCO-C1-C4alkyl, NHCO-C3-C6cycloalkyl, -NHSO2(C1-C4alkyl), -N(C1-C4alkyl)CO-C1-C4alkyl, -N(C1-C4alkyl)CO-C3-C6cyclolkyl, -N(C1-C4alkyl)SO2C1- C4alkyl, -N(SO2C1-C4alkyl)2, -CO2C1-C4alkyl, -CONH(C1-C4alkyl), -CONH(C3-C6cycloalkyl), - CONH-phenyl, -CON(C1-C4alkyl)2, -CON(C1-C4alkyl)(C3-C6cycloalkyl), -CON(C1-C4alkyl)- phenyl, -C(=NOC1-C4alkyl)H, -C(=NOC1-C4alkyl)-C1-C4alkyl, (C1-C4alkyl)3-silyl, -SO2NH(C1- C4alkyl), phenylsulfonyl , or 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein phenyl groups of the aforementioned substituents and the 3- to 6-membered heterocyclyl substituent may optionally carry 1, 2 or 3 substituents independently selected from the group consisting of halogen, CN, C1-C6alkyl, C1-C6haloalkyl and C1-C3cyanoalkyl; and R26 is halogen, -CN, -COOH, -CONH2, -NO2, -SF5, C1-C3alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1- C3haloalkoxy, C1-C3haloalkylthio, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1- C3haloalkylsulfinyl, C1-C3haloalkylsulfonyl, C3-C6cycloalkylsulfanyl, C3-C6cycloalkylsulfinyl, C3-C6cycloalkylsulfonyl, C3-C6cycloalkyl, C1-C3cyanoalkyl, C3-C6cyanocycloalkyl.
10. The compounds according to any one of claims 1 to 8, characterized by having a structure according to formulae (I-vii) - (I-xix)
Figure imgf000279_0001
Figure imgf000280_0001
wherein R1, R3, R5 and R6 have the meaning as defined in any of the preceding claims; R7 are the same or different and have the meaning of the substituents on the phenyl or 5- or 6- membered heteroaryl as defined for R2 in any of the preceding claims; R8 are the same or different and have the meaning of the substituents on the monocyclic heterocycle as defined for R4 in any of the preceding claims; R81 represents in each case optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3- C6cycloalkyl, C1-C3haloalkyl, hydroxy-C2-C4alkyl, -CO2C1-C4alkyl, -C(=NOC1-C4alkyl)H, - C(=NOC1-C4alkyl)-C1-C4alkyl, wherein the aforementioned optionally substituted radicals are optionally substituted with up to 3 substituents independently selected from the group consisting of halogen, hydroxy, -CN, -NO2, -Si(CH3)3, -NH2, C1-C3alkyl, C1-C3haloalkyl, C3-C4cycloalkyl, C3-C4halocycloalkyl, C1-C4alkoxy, C1-C4haloalkoxy, C1-C3alkylsulfonyl, C3- C4cycloalkylsulfonyl, C1-C3haloalkylthio and C1-C3haloalkylsulfonyl; or represents 3- to 6-membered heterocyclyl containing 1 or 2 heteroatoms selected from the group consisting of N, O, and S, wherein the 3- to 6-membered heterocyclyl may optionally carry 1, 2, 3 or 4 substituents independently selected from the group consisting of halogen, hydroxy, CN, -COOH, -CONH2, -CSNH2, -NO2, -Si(CH3)3, -SF5, -NH2, C1-C6alkyl, C3-C6cycloalkyl, C3- C6cyanocycloalkyl, C3-C6halocycloalkyl, C3-C6cycloalkyl- C1-C6alkyl, C1-C3haloalkyl, C1- C3cyanoalkyl, C1-C4alkoxy, C1-C3haloalkoxy, C1-C3cyanoalkoxy, C1-C3alkylthio, C1- C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3haloalkylthio, C1-C3haloalkylsulfinyl, C1- C3haloalkylsulfonyl, C1-C3cyanoalkylthio, C1-C3cyanoalkylsulfinyl, C1-C3cyanoalkylsulfonyl; n represents an integer of 0, 1 or 2; m represents an integer of 1 or 2; and salts and N-oxides thereof.
11. Formulation comprising at least one compound of the formula (I) according to any of claims 1 to 10, and which may further comprise at least one further compound selected from extenders, surface-active substances, auxiliaries, excipients, solvents and/or additional pharmaceutically active agents.
12. The compounds of the formula (I) according to any of claims 1 to 10 or a formulation according to claim 9 for the use as a medicament.
13. The compounds of the formula (I) according to any of claims 1 to 10 or a formulation according to claim 9 for the use as an antiendoparasitical agent, as an antiectoparasitical agent, as an arthropodicidal agent, as an insecticidal agent or as an acaricidal agent.
14. Use of a compound of the formula (I) according to any of claims 1 to 10 or of a formulation according to claim 9 for controlling animal pests or in the field of animal health, wherein methods for treatment of the animal body by surgery or therapy and diagnostic methods practised on the animal body are excluded, or for crop protection, or in vector control, wherein preferably the animal pest comprises an insect, or an arachnid, or in that the animal pest is an insect, or an arachnid .
15. Method for controlling pests, especially animal pests, characterized in that a compound of the formula (I) according to any of claims 1 to 10 or a formulation according to claim 11 is allowed to act on the pests and/or their habitat, wherein methods for treatment of the animal body by surgery or therapy and diagnostic methods practised on the animal body are excluded; or for protecting seed or a germinating plant from pests, especially animal pests, comprising a method step in which the seed is contacted with a compound of the formula (I) according to any of claims 1 to 8 or with a formulation according to claim 9; wherein in said methods the pest is preferably selected from an animal pest selected from the group consisting of insects, and arachnids.
16. Seed obtained by a method according to claim 15.
17. Intermediate Compounds according to formula IX-1, X or XIII
Figure imgf000282_0001
wherein R3, R4, R5 and R6 have the meaning as defined in any of the claims 1 to 8.
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* Cited by examiner, † Cited by third party
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WO2022268648A1 (en) 2021-06-24 2022-12-29 Syngenta Crop Protection Ag 2-[3-[1 [(quinazolin-4-yl)amino]ethyl]pyrazin-2-yl]thiazole-5-carbonitrile derivatives and similar compounds as pesticides
EP4140986A1 (en) 2021-08-23 2023-03-01 Basf Se Pyrazine compounds for the control of invertebrate pests
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EP4151631A1 (en) 2021-09-20 2023-03-22 Basf Se Heterocyclic compounds for the control of invertebrate pests
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EP4194453A1 (en) 2021-12-08 2023-06-14 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023104564A1 (en) 2021-12-08 2023-06-15 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023247360A1 (en) 2022-06-21 2023-12-28 Syngenta Crop Protection Ag Pesticidally active fused bicyclic heteroaromatic compounds
WO2024022910A1 (en) 2022-07-26 2024-02-01 Syngenta Crop Protection Ag 1-[1-[2-(pyrimidin-4-yl)-1,2,4-triazol-3-yl]ethyl]-3-[2,4-dichloro-5-phenyl]urea derivatives and similar compounds as pesticides
EP4389210A1 (en) * 2022-12-21 2024-06-26 Basf Se Heteroaryl compounds for the control of invertebrate pests
WO2024132636A1 (en) * 2022-12-21 2024-06-27 Basf Se Heteroaryl compounds for the control of invertebrate pests
WO2024133551A1 (en) 2022-12-21 2024-06-27 Syngenta Crop Protection Ag Pesticidally active pyridazine compounds

Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003106457A1 (en) 2002-06-14 2003-12-24 Syngenta Limited Spiroindolinepiperidine derivatives
WO2004099160A1 (en) 2003-05-12 2004-11-18 Sumitomo Chemical Company, Limited Pyrimidine compounds and pests controlling composition containing the same
WO2006003494A2 (en) 2004-06-28 2006-01-12 Syngenta Participations Ag Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides
WO2006043635A1 (en) 2004-10-20 2006-04-27 Kumiai Chemical Industry Co., Ltd. 3-triazolylphenyl sulfide derivative and insecticide/acaricide/nematicide containing the same as active ingredient
WO2007040282A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Bridged cyclic amine compound and pest control agent
CN101337940A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 Nitrogen heterocyclic ring dichlorin allyl ether compounds with insecticidal activity
CN101337937A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 N-benz-3-substituted amino pyrazoles compounds with insecticidal activity
JP2010018586A (en) 2008-07-14 2010-01-28 Meiji Seika Kaisha Ltd Substance pf1364, its manufacturing method, producing strain and agricultural/horticultural insecticide having the substance as active ingredient
WO2010052161A2 (en) 2008-11-06 2010-05-14 Syngenta Participations Ag Herbicidal compositions
WO2010051926A2 (en) 2008-11-05 2010-05-14 Bayer Cropscience Aktiengesellschaft New halogen-substituted bonds
CN101715774A (en) 2008-10-09 2010-06-02 浙江化工科技集团有限公司 Preparation and use of compound having insecticidal activity
WO2010066780A1 (en) 2008-12-12 2010-06-17 Syngenta Participations Ag Spiroheterocyclic n-oxypiperidines as pesticides
WO2011067272A1 (en) 2009-12-01 2011-06-09 Syngenta Participations Ag Insecticidal compounds based on isoxazoline derivatives
WO2011085575A1 (en) 2010-01-15 2011-07-21 江苏省农药研究所股份有限公司 Ortho-heterocyclyl formanilide compounds, their synthesis methods and use
WO2011151146A1 (en) 2010-05-31 2011-12-08 Syngenta Participations Ag Method of crop enhancement
WO2012034403A1 (en) 2010-09-14 2012-03-22 中化蓝天集团有限公司 Fluoromethoxypyrazole anthranilamide compounds, synthesization methods and uses thereof
CN102391261A (en) 2011-10-14 2012-03-28 上海交通大学 N-substituted dioxazine compound as well as preparation method and application thereof
WO2013050302A1 (en) 2011-10-03 2013-04-11 Syngenta Participations Ag Isoxazoline derivatives as insecticidal compounds
WO2013050317A1 (en) 2011-10-03 2013-04-11 Syngenta Limited Polymorphs of an isoxazoline derivative
CN103109816A (en) 2013-01-25 2013-05-22 青岛科技大学 Thiobenzamide compounds and application thereof
CN103232431A (en) 2013-01-25 2013-08-07 青岛科技大学 Dihalogenated pyrazole amide compound and its use
WO2013115391A1 (en) 2012-02-01 2013-08-08 日本農薬株式会社 Arylalkyloxy pyrimidine derivative, pesticide for agricultural and horticultural use containing arylalkyloxy pyrimidine derivative as active ingredient, and use of same
CN103265527A (en) 2013-06-07 2013-08-28 江苏省农用激素工程技术研究中心有限公司 Anthranilamide compound as well as preparation method and application thereof
WO2013144213A1 (en) 2012-03-30 2013-10-03 Basf Se N-substituted pyridinylidene compounds and derivatives for combating animal pests
EP2647626A1 (en) 2012-04-03 2013-10-09 Syngenta Participations AG. 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides
WO2013162716A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
CN103524422A (en) 2013-10-11 2014-01-22 中国农业科学院植物保护研究所 Benzimidazole derivative, and preparation method and purpose thereof
US20140213448A1 (en) 2012-04-27 2014-07-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
US20140275503A1 (en) 2013-03-13 2014-09-18 Dow Agrosciences Llc Process for the preparation of certain triaryl rhamnose carbamates
WO2014187846A1 (en) 2013-05-23 2014-11-27 Syngenta Participations Ag Tank-mix formulations
WO2015058021A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2015058028A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2017192385A1 (en) 2016-05-05 2017-11-09 Elanco Tiergesundheit Ag Heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compounds for controlling ectoparasites
WO2019170626A1 (en) 2018-03-08 2019-09-12 Bayer Aktiengesellschaft Use of heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides in plant protection
WO2019197468A1 (en) 2018-04-12 2019-10-17 Bayer Aktiengesellschaft N-(cyclopropylmethyl)-5-(methylsulfonyl)-n-{1-[1-(pyrimidin-2-yl)-1h-1,2,4-triazol-5-yl]ethyl}benzamide derivatives and the corresponding pyridine-carboxamide derivatives as pesticides
WO2019201835A1 (en) 2018-04-17 2019-10-24 Bayer Aktiengesellschaft Heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019202077A1 (en) 2018-04-20 2019-10-24 Bayer Aktiengesellschaft Heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019206799A1 (en) 2018-04-25 2019-10-31 Bayer Aktiengesellschaft Novel heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019215198A1 (en) 2018-05-08 2019-11-14 Syngenta Crop Protection Ag Methods of applying one or more certain heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compounds to control damage on plants, propagation material thereof, and plant derived products
WO2020002563A1 (en) 2018-06-29 2020-01-02 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020053364A1 (en) 2018-09-13 2020-03-19 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020053365A2 (en) 2018-09-13 2020-03-19 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020070049A1 (en) 2018-10-02 2020-04-09 Syngenta Participations Ag Pesticidally active benzene- and azine-amide compounds
WO2020079198A1 (en) 2018-10-19 2020-04-23 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020169445A1 (en) 2019-02-18 2020-08-27 Syngenta Crop Protection Ag Pesticidally active azole-amide compounds
WO2020201398A1 (en) * 2019-04-05 2020-10-08 Syngenta Crop Protection Ag Pesticidally active diazine-amide compounds
WO2020208036A1 (en) * 2019-04-11 2020-10-15 Syngenta Crop Protection Ag Pesticidally active diazine-amide compounds

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5030945B2 (en) * 2005-05-03 2012-09-19 バイエル・クロップサイエンス・アーゲー New heterocyclylethylbenzamide derivatives
JP2009023994A (en) * 2007-06-21 2009-02-05 Nippon Nohyaku Co Ltd Agricultural and horticultural bactericide composition and usage thereof
JP2011178673A (en) * 2010-02-26 2011-09-15 Nissan Chem Ind Ltd Control method for non-agricultural/horticultural insect pest
CN114269732A (en) * 2019-08-23 2022-04-01 先正达农作物保护股份公司 Pesticidally active pyrazine-amide compounds

Patent Citations (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003106457A1 (en) 2002-06-14 2003-12-24 Syngenta Limited Spiroindolinepiperidine derivatives
WO2004099160A1 (en) 2003-05-12 2004-11-18 Sumitomo Chemical Company, Limited Pyrimidine compounds and pests controlling composition containing the same
WO2006003494A2 (en) 2004-06-28 2006-01-12 Syngenta Participations Ag Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides
WO2006043635A1 (en) 2004-10-20 2006-04-27 Kumiai Chemical Industry Co., Ltd. 3-triazolylphenyl sulfide derivative and insecticide/acaricide/nematicide containing the same as active ingredient
WO2007040282A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Bridged cyclic amine compound and pest control agent
WO2007040280A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Cyclic amine compound and pest control agent
JP2010018586A (en) 2008-07-14 2010-01-28 Meiji Seika Kaisha Ltd Substance pf1364, its manufacturing method, producing strain and agricultural/horticultural insecticide having the substance as active ingredient
CN101337940A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 Nitrogen heterocyclic ring dichlorin allyl ether compounds with insecticidal activity
CN101337937A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 N-benz-3-substituted amino pyrazoles compounds with insecticidal activity
CN101715774A (en) 2008-10-09 2010-06-02 浙江化工科技集团有限公司 Preparation and use of compound having insecticidal activity
WO2010051926A2 (en) 2008-11-05 2010-05-14 Bayer Cropscience Aktiengesellschaft New halogen-substituted bonds
WO2010052161A2 (en) 2008-11-06 2010-05-14 Syngenta Participations Ag Herbicidal compositions
WO2010066780A1 (en) 2008-12-12 2010-06-17 Syngenta Participations Ag Spiroheterocyclic n-oxypiperidines as pesticides
WO2011067272A1 (en) 2009-12-01 2011-06-09 Syngenta Participations Ag Insecticidal compounds based on isoxazoline derivatives
WO2011085575A1 (en) 2010-01-15 2011-07-21 江苏省农药研究所股份有限公司 Ortho-heterocyclyl formanilide compounds, their synthesis methods and use
WO2011151146A1 (en) 2010-05-31 2011-12-08 Syngenta Participations Ag Method of crop enhancement
WO2012034403A1 (en) 2010-09-14 2012-03-22 中化蓝天集团有限公司 Fluoromethoxypyrazole anthranilamide compounds, synthesization methods and uses thereof
WO2013050302A1 (en) 2011-10-03 2013-04-11 Syngenta Participations Ag Isoxazoline derivatives as insecticidal compounds
WO2013050317A1 (en) 2011-10-03 2013-04-11 Syngenta Limited Polymorphs of an isoxazoline derivative
CN102391261A (en) 2011-10-14 2012-03-28 上海交通大学 N-substituted dioxazine compound as well as preparation method and application thereof
WO2013115391A1 (en) 2012-02-01 2013-08-08 日本農薬株式会社 Arylalkyloxy pyrimidine derivative, pesticide for agricultural and horticultural use containing arylalkyloxy pyrimidine derivative as active ingredient, and use of same
WO2013144213A1 (en) 2012-03-30 2013-10-03 Basf Se N-substituted pyridinylidene compounds and derivatives for combating animal pests
EP2647626A1 (en) 2012-04-03 2013-10-09 Syngenta Participations AG. 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides
WO2013162716A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
WO2013162715A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
US20140213448A1 (en) 2012-04-27 2014-07-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
CN103232431A (en) 2013-01-25 2013-08-07 青岛科技大学 Dihalogenated pyrazole amide compound and its use
CN103109816A (en) 2013-01-25 2013-05-22 青岛科技大学 Thiobenzamide compounds and application thereof
US20140275503A1 (en) 2013-03-13 2014-09-18 Dow Agrosciences Llc Process for the preparation of certain triaryl rhamnose carbamates
WO2014187846A1 (en) 2013-05-23 2014-11-27 Syngenta Participations Ag Tank-mix formulations
CN103265527A (en) 2013-06-07 2013-08-28 江苏省农用激素工程技术研究中心有限公司 Anthranilamide compound as well as preparation method and application thereof
CN103524422A (en) 2013-10-11 2014-01-22 中国农业科学院植物保护研究所 Benzimidazole derivative, and preparation method and purpose thereof
WO2015058021A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2015058028A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2017192385A1 (en) 2016-05-05 2017-11-09 Elanco Tiergesundheit Ag Heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compounds for controlling ectoparasites
WO2019170626A1 (en) 2018-03-08 2019-09-12 Bayer Aktiengesellschaft Use of heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides in plant protection
WO2019197468A1 (en) 2018-04-12 2019-10-17 Bayer Aktiengesellschaft N-(cyclopropylmethyl)-5-(methylsulfonyl)-n-{1-[1-(pyrimidin-2-yl)-1h-1,2,4-triazol-5-yl]ethyl}benzamide derivatives and the corresponding pyridine-carboxamide derivatives as pesticides
WO2019201835A1 (en) 2018-04-17 2019-10-24 Bayer Aktiengesellschaft Heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019202077A1 (en) 2018-04-20 2019-10-24 Bayer Aktiengesellschaft Heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019206799A1 (en) 2018-04-25 2019-10-31 Bayer Aktiengesellschaft Novel heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides
WO2019215198A1 (en) 2018-05-08 2019-11-14 Syngenta Crop Protection Ag Methods of applying one or more certain heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compounds to control damage on plants, propagation material thereof, and plant derived products
WO2020002563A1 (en) 2018-06-29 2020-01-02 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020053364A1 (en) 2018-09-13 2020-03-19 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020053365A2 (en) 2018-09-13 2020-03-19 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020070049A1 (en) 2018-10-02 2020-04-09 Syngenta Participations Ag Pesticidally active benzene- and azine-amide compounds
WO2020079198A1 (en) 2018-10-19 2020-04-23 Syngenta Participations Ag Pesticidally active azole-amide compounds
WO2020169445A1 (en) 2019-02-18 2020-08-27 Syngenta Crop Protection Ag Pesticidally active azole-amide compounds
WO2020201398A1 (en) * 2019-04-05 2020-10-08 Syngenta Crop Protection Ag Pesticidally active diazine-amide compounds
WO2020208036A1 (en) * 2019-04-11 2020-10-15 Syngenta Crop Protection Ag Pesticidally active diazine-amide compounds

Non-Patent Citations (13)

* Cited by examiner, † Cited by third party
Title
"FAO Plant Production and Protection Papers", vol. 173, 2004, FAO/WHO JOINT MEETING ON PESTICIDE SPECIFICATIONS, article "Crop Life International and in Pesticide Specifications"
"The Pesticide Manual", 2012, BRITISH CROP PROTECTION COUNCIL
BAUR ET AL., PESTICIDE SCIENCE, vol. 51, 1997, pages 131 - 152
CAS , no. 1309959-62-3
CAS, no. 885026-50-6
F. BURONN. PIEA. TURCKG, QUEGUIGNER, J. ORG. CHEM., vol. 70, 2005, pages 2616 - 2621
G.R. DICKD.M. KNAPPE.P. GILLISM.D. BURKE, ORG. LETT., vol. 12, 2010, pages 2314 - 2317
HUNT ET AL., MED. VET. ENTOMOL., vol. 19, no. 3, September 2005 (2005-09-01), pages 271 - 275
M.R. LUZUNGJ.S. PATELJ. YIN, J. ORG. CHEM., vol. 75, 2010, pages 8330 - 8332
R. MARTINS.L. BUCHWALD, ACC. CHEM. RES., vol. 61, 2008, pages 1461 - 1473
R. WEGLER: "Chemie der Pflanzenschutz- and Schadlingsbekampfungsmittel", vol. 2, 1970, SPRINGER VERLAG, pages: 401 - 412
T. KLATTJ.T. MARKIEWICZC. SAMANNP. KNOCHEL, J. ORG. CHEM., vol. 79, 2014, pages 4253 - 4269
T.W. GREENEP.G.M. WUTS: "Protective Groups in Organic Chemistry", 1999, WILEY INTERSCIENCE

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EP4140986A1 (en) 2021-08-23 2023-03-01 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023025602A1 (en) 2021-08-23 2023-03-02 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023025682A1 (en) 2021-08-25 2023-03-02 Bayer Aktiengesellschaft Novel pyrazinyl-triazole compounds as pesticides
EP4140995A1 (en) 2021-08-27 2023-03-01 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023025617A1 (en) 2021-08-27 2023-03-02 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023041422A1 (en) 2021-09-20 2023-03-23 Basf Se Heterocyclic compounds for the control of invertebrate pests
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WO2023104564A1 (en) 2021-12-08 2023-06-15 Basf Se Pyrazine compounds for the control of invertebrate pests
WO2023247360A1 (en) 2022-06-21 2023-12-28 Syngenta Crop Protection Ag Pesticidally active fused bicyclic heteroaromatic compounds
WO2024022910A1 (en) 2022-07-26 2024-02-01 Syngenta Crop Protection Ag 1-[1-[2-(pyrimidin-4-yl)-1,2,4-triazol-3-yl]ethyl]-3-[2,4-dichloro-5-phenyl]urea derivatives and similar compounds as pesticides
EP4389210A1 (en) * 2022-12-21 2024-06-26 Basf Se Heteroaryl compounds for the control of invertebrate pests
WO2024132636A1 (en) * 2022-12-21 2024-06-27 Basf Se Heteroaryl compounds for the control of invertebrate pests
WO2024133551A1 (en) 2022-12-21 2024-06-27 Syngenta Crop Protection Ag Pesticidally active pyridazine compounds

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